C. Stoll

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Lifetime intellectual function and satisfaction with life in old age: longitudinal cohort study

F. Bianchi, N. Baena, R. Caballín, 2005 .

Genetic and environmental factors in hypospadias.

C. Stoll, Y. Alembik, M. Roth, 1990, Journal of medical genetics.

International retrospective cohort study of neural tube defects in relation to folic acid recommendations: are the recommendations working?

S. Vollset, M. Feijóo, G. Scarano, 2005, BMJ : British Medical Journal.

Limb reduction defects in the first generation and deafness in the second generation of intrauterine exposed fetuses to diethylstilbestrol.

C. Stoll, Y. Alembik, B. Dott, 2003, Annales de genetique.

Prenatal diagnosis of dysmorphic syndromes by routine fetal ultrasound examination across Europe

C. Stoll, M. Clementi, 2003, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Evaluation of the prenatal diagnosis of neural tube defects by fetal ultrasonographic examination in different centres across Europe

R. Tenconi, C. Stoll, M. Clementi, 2000, Journal of medical screening.

Prenatal diagnosis of congenital my asthenia with arthrogryposis in a myasthenic mother

C. Stoll, C. Tranchant, A. Treisser, 1991, Prenatal diagnosis.

Associated malformations in patients with esophageal atresia.

C. Stoll, Y. Alembik, M. Roth, 2009, European journal of medical genetics.

Prenatal detection of rare chromosomal autosomal abnormalities in Europe

N. Baena, C. Stoll, M. Clementi, 2003, American journal of medical genetics. Part A.

Twelve cases with hemihypertrophy: etiology and follow up.

C. Stoll, Y. Alembik, A. de Saint-Martin, 1993, Genetic counseling.

Associated anomalies in cases with esophageal atresia

C. Stoll, Y. Alembik, M. Roth, 2017, American journal of medical genetics. Part A.

Birth prevalence rates of skeletal dysplasias

C. Stoll, Y. Alembik, M. Roth, 1989, Clinical genetics.

Parental consanguinity as a cause of increased incidence of birth defects in a study of 131,760 consecutive births.

C. Stoll, J. Feingold, Y. Alembik, 1994, American journal of medical genetics.

Trends and geographic inequalities in the prevalence of Down syndrome in Europe, 1980-1999.

F. Bianchi, M. Loane, M. Feijóo, 2005, Revue d'epidemiologie et de sante publique.

Trends of selected malformations in relation to folic acid recommendations and fortification: an international assessment.

C. Stoll, P. Mastroiacovo, L. Irgens, 2006, Birth defects research. Part A, Clinical and molecular teratology.

Impact of prenatal diagnosis on livebirth prevalence of children with congenital anomalies.

C. Stoll, Y. Alembik, M. Roth, 2002, Annales de genetique.

Turner syndrome: Evaluation of prenatal diagnosis in 19 European registries

N. Baena, C. Stoll, M. Clementi, 2004, American journal of medical genetics. Part A.

Paternal age and Down's syndrome diagnosed prenatally: No association in French data

C. Stoll, M. Roth, A. Boué, 1983, Prenatal diagnosis.

Severe hypernatremic dehydration in an infant with Netherton syndrome.

C. Stoll, P. Calvas, A. Hovnanian, 2001, Genetic counseling.

Associated anomalies in cases with agenesis of the corpus callosum

C. Stoll, M. Roth, B. Dott, 2019, American journal of medical genetics. Part A.

Associated noncardiac congenital anomalies among cases with congenital heart defects.

C. Stoll, Y. Alembik, M. Roth, 2015, European journal of medical genetics.

Study of Down syndrome in 238,942 consecutive births.

C. Stoll, Y. Alembik, M. Roth, 1998, Annales de genetique.

Sex and congenital malformations: An international perspective

F. Bianchi, G. Scarano, C. Stoll, 2005, American journal of medical genetics. Part A.

Congenital diaphragmatic hernia: evaluation of prenatal diagnosis in 20 European regions

E. Garne, M. Haeusler, C. Stoll, 2002, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Growth curves of children with Down syndrome.

C. Stoll, Y. Alembik, A. Aguirre Jaime, 1999, Annales de genetique.

An epidemiologic study of environmental and genetic factors in congenital hydrocephalus

C. Stoll, Y. Alembik, M. Roth, 1992, European Journal of Epidemiology.

Discordance for skeletal and cardiac defect in monozygotic twins.

C. Stoll, M. Roth, B. Dott, 1984, Acta geneticae medicae et gemellologiae.

SIMPLE mutation analysis in dominant demyelinating Charcot‐Marie‐Tooth disease: three novel mutations

C. Stoll, P. Latour, T. Stojkovic, 2006, Journal of the peripheral nervous system : JPNS.

Prenatal diagnosis of a lethal form of Netherton syndrome by SPINK5 mutation analysis

C. Bodemer, C. Stoll, P. Calvas, 2002, Prenatal diagnosis.

The spectrum of congenital anomalies of the VATER association: an international study.

M. Khoury, C. Stoll, C. Moore, 1997, American journal of medical genetics.

Tyrosine hydroxylase deficiency unresponsive to L-dopa treatment with unusual clinical and biochemical presentation

C. Stoll, R. Wevers, J. Launay, 2000, Journal of Inherited Metabolic Disease.

Associated malformations in cases with neural tube defects.

C. Stoll, Y. Alembik, B. Dott, 2007, Genetic counseling.

Evaluation of prenatal diagnosis of congenital heart disease

C. Stoll, Y. Alembik, B. Dott, 1993, Prenatal diagnosis.

Evaluation of routine prenatal ultrasound examination in detecting fetal chromosomal abnormalities in a low risk population

C. Stoll, Y. Alembik, M. Roth, 1993, Human Genetics.

Contribution of ultrasonographic examination to the prenatal detection of chromosomal abnormalities in 19 centres across Europe.

N. Baena, C. Stoll, M. Clementi, 2001, Annales de genetique.

Epidemiology of Down syndrome in 118,265 consecutive births.

C. Stoll, Y. Alembik, M. Roth, 2005, American journal of medical genetics. Supplement.

Familial coarctation of the aorta in three generations.

C. Stoll, Y. Alembik, B. Dott, 1999, Annales de genetique.

Prenatal diagnosis of severe structural congenital malformations in Europe

M. Loane, M. Feijóo, E. Garne, 2005, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Detection of Congenital Anomalies by Fetal Ultrasonographic Examination across Europe

R. Tenconi, C. Stoll, M. Clementi, 2002, Public Health Genomics.

Prevalence of neural tube defects in northeastern France, 1979-1994. Impact of prenatal diagnosis.

C. Stoll, Y. Alembik, M. Roth, 1997, Annales de genetique.

HLA and down syndrome (DS): Parents at the origin of the nondisjunction share no more HLA‐A and ‐B antigens with their DS child than controls

C. Stoll, D. Rao, S. Mayer, 1988, Genetic epidemiology.

Hereditary renal adysplasia in a three generations family.

C. Stoll, B. Gasser, B. Doray, 1999, Genetic counseling.

Evaluation and evolution during time of prenatal diagnosis of congenital heart diseases by routine fetal ultrasonographic examination.

C. Stoll, Y. Alembik, B. Dott, 2002, Annales de genetique.

International retrospective cohort study of neural tube defects in relation to folic acid recommendations: are the recommendations working?

S. Vollset, M. Feijóo, G. Scarano, 2005, BMJ : British Medical Journal.

Co‐occurring anomalies in congenital oral clefts

C. Stoll, Y. Alembik, M. Roth, 2022, American journal of medical genetics. Part A.

Associated anomalies in cases with congenital clubfoot.

C. Stoll, M. Roth, B. Dott, 2020, American journal of medical genetics. Part A.

Associated anomalies in cases with anorectal anomalies

C. Stoll, Y. Alembik, M. Roth, 2018, American journal of medical genetics. Part A.

Associated anomalies in cases with anotia and microtia.

C. Stoll, Y. Alembik, M. Roth, 2016, European journal of medical genetics.

Evaluation of prenatal ultrasound diagnosis of fetal abdominal wall defects by 19 European registries

C. Stoll, M. Clementi, M. Häusler, 2001, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Shprintzen-Goldberg marfanoid syndrome: a case followed up for 24 years.

C. Stoll, 2002, Clinical dysmorphology.

Prevalence of neural tube defects in northeastern France, 1979-1992 impact of prenatal diagnosis.

C. Stoll, Y. Alembik, M. Roth, 1995, Annales de genetique.

Acetylator phenotype and congenital malformations

C. Stoll, J. Imbs, Y. Alembik, 2004, European Journal of Clinical Pharmacology.

Congenital eye malformations in 212,479 consecutive births.

C. Stoll, Y. Alembik, M. Roth, 1997, Annales de genetique.

Epidemiology of congenital eye malformations in 131,760 consecutive births.

C. Stoll, Y. Alembik, M. Roth, 1992, Ophthalmic paediatrics and genetics.

Evaluation of prenatal diagnosis of associated congenital heart diseases by fetal ultrasonographic examination in Europe

E. Garne, C. Stoll, M. Clementi, 2001, Prenatal diagnosis.

Routine fetal echocardiography and detection of congenital heart disease

C. Stoll, Y. Alembik, 1996, The Lancet.

Associated malformations in cases with congenital diaphragmatic hernia.

C. Stoll, Y. Alembik, M. Roth, 2008, Genetic counseling.

Omphalocele and gastroschisis and associated malformations

C. Stoll, Y. Alembik, M. Roth, 2008, American journal of medical genetics. Part A.

Progressive osseous heteroplasia: an uncommon cause of ossification of soft tissues.

C. Stoll, J. Bellocq, C. Stoll, 2000, Annales de genetique.

Co‐occurring non‐omphalocele and non‐gastroschisis anomalies among cases with congenital omphalocele and gastroschisis

C. Stoll, Y. Alembik, M. Roth, 2021, American journal of medical genetics. Part A.

An unusual human mosaic for skin pigmentation.

C. Stoll, Y. Alembik, A. De Saint Martin, 2002, Genetic counseling.

A family with dominant oculoauriculovertebral spectrum.

C. Stoll, B. Gasser, B. Viville, 1998, American journal of medical genetics.

Sister chromatid exchanges in balanced translocation carriers and in patients with unbalanced karyotypes

C. Stoll, D. Borgaonkar, P. Bigel, 1977, Human Genetics.

Associated nonurinary congenital anomalies among infants with congenital anomalies of kidney and urinary tract (CAKUT).

C. Stoll, Y. Alembik, M. Roth, 2014, European journal of medical genetics.

An asymptomatic enlargement of the mandible causing marked root resorption.

C. Stoll, G. Baretton, W. Winter, 1997, Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons.

Associated congenital anomalies among cases with Down syndrome.

C. Stoll, Y. Alembik, M. Roth, 2015, European journal of medical genetics.

Abnormal children of a 47,XYY father.

C. Stoll, E. Flori, A. Clavert, 1979, Journal of medical genetics.

Study of 290 Cases of Polyhydramnios and Congenital Malformations in a Series of 225,669 Consecutive Births

C. Stoll, Y. Alembik, M. Roth, 1999, Public Health Genomics.

Study of 224 Cases of Oligohydramnios and Congenital Malformations in a Series of 225,669 Consecutive Births

C. Stoll, Y. Alembik, M. Roth, 1998, Public Health Genomics.

Associated malformations among infants with neural tube defects

C. Stoll, Y. Alembik, M. Roth, 2011, American journal of medical genetics. Part A.

Prenatal ultrasonographic detection of gastrointestinal obstruction: results from 18 European congenital anomaly registries

A. Berghold, M. Haeusler, C. Stoll, 2002, Prenatal diagnosis.

Hemodynamics and cardiogenesis: the effects of physiologic factors on cardiac development.

C. Stoll, E. Flori, D. Beshara, 1978 .

Interchromosomal effect in balanced translocations.

C. Stoll, E. Flori, D. Beshara, 1978, Birth defects original article series.

Time trends in neural tube defects prevalence in relation to preventive strategies: an international study.

C. Stoll, A. Rosano, M. Cornel, 1999, Journal of epidemiology and community health.

Prenatal sonographic diagnosis of skeletal dysplasias. A report of 47 cases.

C. Stoll, R. Favre, M. Dreyfus, 2000, Annales de genetique.

Prenatal diagnosis of hypochondroplasia

C. Stoll, M. Roth, P. Manini, 1985, Prenatal diagnosis.

Do parents and grandparents of patients with achondroplasia have a higher cancer risk?

C. Stoll, J. Feingold, 2004, American journal of medical genetics. Part A.

Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wide

S. Vollset, E. Bermejo, S. Bianca, 2003, Journal of medical genetics.

No evidence for genomic imprinting in liver-born Down syndrome patients.

C. Stoll, J. Feingold, Y. Alembik, 1996, Acta geneticae medicae et gemellologiae.

Segregation of a 22 ring chromosome in three generations

C. Stoll, M. Roth, 2004, Human Genetics.

Associated malformations among infants with anophthalmia and microphthalmia.

C. Stoll, Y. Alembik, M. Roth, 2012, Birth defects research. Part A, Clinical and molecular teratology.

Study of placenta of children born with congenital malformations.

C. Stoll, Y. Alembik, M. Roth, 2003, Annales de genetique.

Risk factors in internal urinary system malformations

C. Stoll, Y. Alembik, M. Roth, 1990, Pediatric Nephrology.

Associated malformations in patients with anorectal anomalies.

C. Stoll, Y. Alembik, M. Roth, 2007, European journal of medical genetics.

Trisomy 1q24----1q41 in two sibs with an insertion in an inverted chromosome 4.

C. Stoll, M. Roth, B. Dott, 1984, Journal of medical genetics.

Multiple familial lipomatosis with polyneuropathy, an inherited dominant condition.

C. Stoll, M. Truttmann, Y. Alembik, 1996, Annales de genetique.

[Anomalies of thyroid function in children with Down syndrome].

C. Stoll, Y. Alembik, B. Dott, 1997, Archives de pédiatrie.

[Anomalies in thyroid function in children with trisomy 21].

C. Stoll, Y. Alembik, B. Dott, 1989, Journal de genetique humaine.

Paternal age and Down's syndrome diagnosed prenatally: No association in French data

C. Stoll, M. Roth, A. Boué, 1983 .

Laryngeal atresia type III (glottic web) with 22q11.2 microdeletion: report of three patients.

S. Antonarakis, C. Stoll, A. Bottani, 1997, American journal of medical genetics.

Difficulties in the diagnosis of neurofibomatosis-1 in children.

C. Stoll, 2002, American journal of medical genetics.

Prenatal detection of internal urinary system's anomalies

C. Stoll, Y. Alembik, M. Roth, 1995, European Journal of Epidemiology.

Evaluation of prenatal diagnosis of congenital gastro-intestinal atresias

C. Stoll, Y. Alembik, M. Roth, 1996, European Journal of Epidemiology.

Evaluation of the prenatal diagnosis of limb reduction deficiencies

S. Bianca, C. Stoll, M. Clementi, 2000, Prenatal diagnosis.

Evaluation of prenatal diagnosis of limb reduction defects by a registry of congenital anomalies

C. Stoll, Y. Alembik, M. Roth, 1994, Prenatal diagnosis.

Evaluation of prenatal diagnosis of congenital heart disease

C. Stoll, Y. Alembik, B. Dott, 1998, Prenatal diagnosis.

ASSOCIATED NON DIAPHRAGMATIC ANOMALIES AMONG CASES WITH CONGENITAL DIAPHRAGMATIC HERNIA.

C. Stoll, Y. Alembik, M. Roth, 2015, Genetic counseling.

Risk factors in congenital abdominal wall defects (omphalocele and gastroschisi): a study in a series of 265,858 consecutive births.

C. Stoll, Y. Alembik, M. Roth, 2001, Annales de genetique.

A boy with neurofibromatosis 1 and Poland anomaly.

C. Stoll, Y. Alembik, 1994, Genetic counseling.

Associated malformations in cases with oral clefts.

C. Stoll, Y. Alembik, M. Roth, 2000, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Sirenomelia and situs inversus: case report and review of the literature.

C. Stoll, B. Gasser, B. Langer, 1996, Fetal diagnosis and therapy.

Autosomal dominant carpal tunnel syndrome

C. Stoll, D. Maitrot, 1998, Clinical genetics.

Binder syndrome in a mother and her son.

C. Stoll, Y. Alembik, B. Roy-Doray, 1997, Genetic counseling.

Study of 156 cases of polyhydramnios and congenital malformations in a series of 118,265 consecutive births.

C. Stoll, Y. Alembik, B. Dott, 1991, American journal of obstetrics and gynecology.

Hepatic calcifications in a fetus with trisomy 9 that underwent cordocentesis

C. Stoll, B. Gasser, D. Satgé, 1994, Prenatal diagnosis.

Long-term follow-up of a girl with oro-facio-digital syndrome type I due to a mutation in the OFD 1 gene.

C. Stoll, P. Sauvage, 2002, Annales de genetique.

Prenatal detection of congenital renal malformations by fetal ultrasonographic examination: an analysis of 709,030 births in 12 European countries.

S. Bianca, C. Stoll, M. Clementi, 2005, European journal of medical genetics.

Familial pterygium syndrome

C. Stoll, M. Roth, P. Kehr, 1980, Clinical genetics.

Evaluation of prenatal diagnosis of congenital heart diseases by ultrasound: experience from 20 European registries

E. Garne, C. Stoll, M. Clementi, 2001, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Evaluation of prenatal diagnosis by a registry of congenital anomalies

C. Stoll, Y. Alembik, M. Roth, 1992, Prenatal diagnosis.

Non-random clonal evolution in 45 cases of chronic myeloid leukemia.

C. Stoll, F. Oberling, 2008, Leukemia research.

Associated Malformations in Cases with Oral Clefts

C. Stoll, Y. Alembik, M. Roth, 2000 .

The Euroscan study

C. Stoll, M. Clementi, 2001, Ultrasound in Obstetrics and Gynecology.

Prenatal diagnostic procedures used in pregnancies with congenital malformations in 14 regions of Europe

M. Loane, N. Baena, M. Feijóo, 2004, Prenatal diagnosis.

Contribution of ultrasonographic examination to the prenatal detection of trisomy 21: experience from 19 European registers.

N. Baena, C. Stoll, M. Clementi, 2004, Annales de genetique.

Evaluation of routine prenatal diagnosis by a registry of congenital anomalies

C. Stoll, Y. Alembik, M. Roth, 1995, Prenatal diagnosis.

north-eastern France . Alsace , in 207 cases of oral clefts in Epidemiological and genetic study

C. Stoll, Y. Alembik, M. Roth, 2004 .

Epidemiological and genetic study in 207 cases of oral clefts in Alsace, north-eastern France.

C. Stoll, Y. Alembik, M. Roth, 1991, Journal of medical genetics.

A Weaver‐like syndrome with endocrinological abnormalities in a boy and his mother

C. Stoll, M. Roth, B. Dott, 1985, Clinical genetics.

Two cases of Townes-Brocks syndrome.

C. Stoll, B. Langer, B. Doray, 1999, Genetic Counseling.

Evaluation of prenatal diagnosis of cleft lip/palate by foetal ultrasonographic examination.

C. Stoll, Y. Alembik, M. Roth, 2000, Annales de genetique.

Siblings with congenital renal tubular acidosis and nerve deafness

C. Stoll, A. Gentine, J. Geisert, 1996, Clinical genetics.

Renal defects and limb deficiencies in 197 infants: Is it possible to define the “acrorenal syndrome”?

C. Stoll, A. Rosano, P. Mastroiacovo, 2004, American journal of medical genetics. Part A.

Usefulness of a registry of congenital malformations for genetic counseling and prenatal diagnosis

C. Stoll, M. Roth, B. Dott, 1986, Clinical genetics.

[Congenital malformations in a series of 66,068 consecutive births].

C. Stoll, Y. Alembik, M. Roth, 1987, Archives francaises de pediatrie.

Partial 4q duplication due to Inherited der(13),t(4;13)(q26;q34)mat in a girl with a deficiency of Factor X

C. Stoll, M. Roth, 1980, Human Genetics.

[De novo t(3 ; 20) (p 14 ; p 12) translocation in a young girl].

C. Stoll, J. Levy, 1974, Annales de genetique.

Ring chromosome 15:r(15). Identification by R banding

C. Stoll, J. C. Luckel, J. Juif, 2004, Humangenetik.

Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15).

C. Stoll, M. Roth, J. Levy, 1980, Journal of medical genetics.

Effect of vincristine on sister chromatid exchanges of normal human lymphocytes.

C. Stoll, D. Borgaonkar, J. Levy, 1976, Cancer research.

Sister chromatid exchange and growth kinetics in chronic myeloid leukemia.

C. Stoll, F. Oberling, M. Roth, 1982, Cancer research.

Sister chromatid exchange and growth kinetics in chronic myeloid leukemia.

C. Stoll, F. Oberling, M. Roth, 1982, Cancer research.

[22-ring chromosome: identification by controlled heat denaturation].

C. Stoll, A. Rohmer, P. Sauvage, 1973, Annales de genetique.

A study on limb reduction defects in six European regions.

E. Garne, E. Calzolari, C. Stoll, 1996, Annales de genetique.

Usefulness of chromosome catalog in delineating new syndromes.

C. Stoll, D. Borgaonkar, Y. Lacassie, 1976, Birth defects original article series.

Different Policies on Prenatal Ultrasound Screening Programmes and Induced Abortions Explain Regional Variations in Infant Mortality with Congenital Malformations

A. Berghold, E. Garne, C. Stoll, 2001, Fetal Diagnosis and Therapy.

9th international workshop on fragile X syndrome and X-linked mental retardation.

G. Ramakers, D. Nelson, C. Schwartz, 2000, American journal of medical genetics.

Familial cylindromatosis.

C. Stoll, Y. Alembik, E. Grosshans, 2004, Genetic counseling.

Limb defects associated with major congenital anomalies: clinical and epidemiological study from the International Clearinghouse for Birth Defects Monitoring Systems.

M. Khoury, C. Stoll, G. Zampino, 2000, American journal of medical genetics.

Maternal trace elements, vitamin B12, vitamin A, folic acid, and fetal malformations.

C. Stoll, Y. Alembik, B. Dott, 1999, Reproductive toxicology.

Hypertrophic pyloric stenosis associated with X‐linked ichthyosis in two brothers

C. Stoll, M. Roth, E. Grosshans, 1983, Clinical and experimental dermatology.

Risk factors in congenital anal atresias.

C. Stoll, Y. Alembik, M. Roth, 1997, Annales de genetique.

On the symmetry of limb deficiencies among children with multiple congenital anomalies.

M. Khoury, E. Bermejo, C. Stoll, 2001, Annales de genetique.

Congenital bilateral fibular deficiency with facial dysmorphia, brachydactyly and mental retardation in a girl.

C. Stoll, Y. Alembik, M. Repetto, 1998, Genetic Counseling.

Multiple congenital malformations including generalized hypertrichosis with gum hypertrophy in a child exposed to valproic acid in utero.

C. Stoll, J. Messer, C. Gaugler, 2003, Genetic counseling.

Parental consanguinity as a cause for increased incidence of births defects in a study of 238,942 consecutive births.

C. Stoll, Y. Alembik, M. Roth, 1999, Annales de genetique.

Associated malformations in patients with oral clefts

C. Stoll, Y. Alembik, M. Roth, 2007, American journal of medical genetics. Part A.

Dandy-Walker variant malformation, spastic paraplegia, and mental retardation in two sibs.

C. Stoll, Y. Alembik, C. Huber, 1990, American journal of medical genetics.

Evaluation of prenatal diagnosis of cleft lip with or without cleft palate and cleft palate by ultrasound: experience from 20 European registries

F. Bianchi, R. Tenconi, C. Stoll, 2000, Prenatal diagnosis.

Preferential Associations between Oral Clefts and Other Major Congenital Anomalies

Guido Cocchi, Pierpaolo Mastroiacovo, Csaba Siffel, 2008, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Congenital blepharophimosis and ptosis in a mentally retarded girl: a new case of Ohdo syndrome?

C. Stoll, 1999, Genetic counseling.

Sporadic case of dyssegmental dysplasia with antenatal presentation.

C. Stoll, Y. Alembik, B. Gasser, 1998, Genetic counseling.

De novo trisomy 22 due to an extra 22Q-chromosome.

C. Stoll, A. Schnebelen, H. Pécheur, 1997, Annales de genetique.

ASPECTS ETIOLOGIQUES ET EPIDEMIOLOGIQUES DES ANOMALIES DU TUBE NEURAL. ETIOLOGIC AND EPIDEMIOLOGIC ASPECTS OF NEURAL TUBE DEFECTS

C. Stoll, Y. Alembik, M. Roth, 1988 .

Pallister-Hall syndrome with stenosis of the cricoid cartilage and microphallus without hypopituitarism.

C. Stoll, J. Messer, A. De Saint Martin, 2001, Genetic counseling.

Chromosome analysis of spleen and/or lymph nodes of patients with chronic myeloid leukemia (CML).

C. Stoll, F. Oberling, E. Flori, 1978, Blood.

The epidemiology of three serious cardiac defects a joint study between five centres

C. Stoll, G. Cocchi, P. Pradat, 1993, European Journal of Epidemiology.

Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in males.

S. Knight, C. Stoll, J. Mandel, 1996, American journal of human genetics.

Associated malformations among infants with radial ray deficiency.

C. Stoll, Y. Alembik, M. Roth, 2013, Genetic Counseling.

international study Time trends in neural tube defects prevalence in relation to preventive strategies: an

C. Stoll, A. Rosano, M. Cornel, 2005 .

strategies : an international study . Time trends in neural tube defects prevalence in relation to preventive

C. Stoll, El, A. Rosano, 1999 .

Associated malformations in patients with limb reduction deficiencies.

C. Stoll, Y. Alembik, M. Roth, 2010, European journal of medical genetics.

Risk factors in limb reduction defects.

C. Stoll, Y. Alembik, M. Roth, 1992, Paediatric and perinatal epidemiology.

[Dubowitz's syndrome].

C. Stoll, P. Buck, J. Levy, 1980, Pediatrie.

Oto-palato-digital syndrome type II.

C. Stoll, Y. Alembik, 1994, Genetic counseling.

A syndrome of congenital ichthyosis, hypogonadism, small stature, facial dysmorphism, scoliosis and myogenic dystrophy.

C. Stoll, D. Eyer, 1999, Annales de genetique.

X deletion and primary amenorrhoea.

C. Stoll, P. Dellenbach, P. Muller, 1973, Lancet.

Recent trends in the prevalence of Down syndrome in north-eastern France.

C. Stoll, Y. Alembik, M. Roth, 1994, Annales de genetique.

Evaluation of prenatal diagnosis of cleft lip with or without cleft palate and cleft palate by ultrasound: experience from 20 European registries

F. Bianchi, R. Tenconi, C. Stoll, 2000, Prenatal diagnosis.

[A case of trisomy 18 with bilateral aplasia of the radius and thrombopenia].

C. Stoll, R. Sacrez, D. Willard, 1972, Pediatrie.

Distribution of single organ malformations in European populations. EUROCAT Working Group.

E. Calzolari, C. Stoll, H. Dolk, 1995, Annales de genetique.

Associated anomalies in cases with achondroplasia.

C. Stoll, Y. Alembik, M. Roth, 2022, European journal of medical genetics.

Associated anomalies in Pierre Robin sequence

C. Stoll, M. Roth, Y. Alembick, 2023, American journal of medical genetics. Part A.

Rett-like syndrome in fragile X syndrome.

C. Stoll, Y. Alembik, B. Dott, 1995, Genetic counseling.

Problems in the diagnosis of fragile X syndrome in young children are still present.

C. Stoll, 2001, American journal of medical genetics.

[Central thyroid insufficiency in the 47, XYY syndrome].

C. Stoll, J. Kupferberg, J. Levy, 1975, Pediatrie.

EVALUATION OF PRENATAL DIAGNOSIS OF CONGENITAL HEART DISEASE

C. Stoll, Y. Alembik, B. Dott, 2022 .

Congenital anomalies associated with congenital hypothyroidism.

C. Stoll, Y. Alembik, B. Dott, 1999, Annales de genetique.

[Etiologic and epidemiologic aspects of neural tube defects].

C. Stoll, Y. Alembik, M. Roth, 1988, Archives francaises de pediatrie.

Risk factors in congenital heart disease

C. Stoll, Y. Alembik, M. Roth, 1989, European Journal of Epidemiology.

Reply to Newton Freire-Maia on inbreeding among medical geneticists II.

C. Stoll, J. Feingold, Y. Alembik, 1995, American journal of medical genetics.

Associated anomalies in cases with anotia and microtia.

C. Stoll, Y. Alembik, M. Roth, 2016, European Journal of Medical Genetics.

Preferential Associations between Oral Clefts and Other Major Congenital Anomalies

E. Bermejo, G. Scarano, C. Stoll, 2008, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Macrocephaly-cutis marmorata telangiectatica congenita: report of a patient with a translocation.

C. Stoll, 2003, Genetic counseling.

working? recommendations: are the recommendations neural tube defects in relation to folic acid International retrospective cohort study of

S. Vollset, C. Stoll, P. Mastroiacovo, 2005 .