E. Passarge

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The Human Karyotype Analysis of Chromosomes in Mitosis and Evaluation of Cytogenetic Data

E. Passarge, 1974 .

R. Farber, B. Horsthemke, E. Passarge, 1999, Nature Genetics.

Constitutional chromothripsis rearrangements involve clustered double-stranded DNA breaks and nonhomologous repair mechanisms.

Markus J. van Roosmalen, E. Cuppen, E. van Binsbergen, 2012, Cell reports.

Transcriptional regulator PRDM12 is essential for human pain perception

David L. Bennett, Andreas C. Themistocleous, I. Katona, 2015, Nature Genetics.

Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastoma

B. Horsthemke, E. Passarge, V. Greger, 1989, Human Genetics.

Emil Heitz and the concept of heterochromatin: longitudinal chromosome differentiation was recognized fifty years ago.

E. Passarge, 1979, American journal of human genetics.

Syndrome of cystic eyelids, palmo-plantar keratosis, hypodontia and hypotrichosis as a possible autosomal recessive trait.

E. Passarge, E. Schöpf, H. Schulz, 1971, Birth defects original article series.

Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome

Sebastian Bauer, Sebastian Köhler, Christian Rödelsperger, 2010, Nature Genetics.

DNA methylation based testing of 450 patients suspected of having Prader-Willi syndrome.

B. Horsthemke, G. Gillessen‐kaesbach, E. Passarge, 1995, Journal of medical genetics.

Marfan syndrome with neonatal progeroid syndrome‐like lipodystrophy associated with a novel frameshift mutation at the 3′ terminus of the FBN1‐gene

P. Robinson, R. Fahsold, L. Graul-Neumann, 2010, American journal of medical genetics. Part A.

Gastrointestinal Tract and Hepatobiliary Duct System

E. Passarge, 2020, Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics.

Marfanoid–progeroid–lipodystrophy syndrome: a newly recognized fibrillinopathy

P. Robinson, L. Graul-Neumann, E. Passarge, 2016, European Journal of Human Genetics.

Somatic mosaicism in a patient with bilateral retinoblastoma.

B. Horsthemke, E. Passarge, V. Greger, 1990, American journal of human genetics.

Bloom's syndrome: the German experience.

E. Passarge, 1991, Annales de genetique.

Gastrointestinal Tract: Molecular Genetics of Hirschsprung Disease

E. Passarge, 2011 .

Genotype-phenotype correlation in a series of 167 deletion and non-deletion patients with Prader-Willi syndrome

B. Horsthemke, D. Lohmann, W. Robinson, 1995, Human Genetics.

Cytogenetic and Clinical Significance of Fragile Sites on Human Chromosomes

E. Passarge, A. Schmidt, 1985 .

Unexpected Angelman syndrome molecular defect in a girl displaying clinical features of Prader-Willi syndrome

G. Gillessen‐kaesbach, E. Passarge, G. Gillessen‐Kaesbach, 1999 .

Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences.

B. Horsthemke, E. Passarge, G. Senger, 1990, Genomics.

Gastrointestinal Tract and Hepatobiliary Duct System

E. Passarge, 2020, Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics.

Letter: Genetic heterogeneity recognized by Waardenburgh in 1935.

E. Passarge, 1976, American journal of human genetics.

In memoriam James L. German, a pioneer in early human genetic research

J. Groden, E. Passarge, 2018, American journal of medical genetics. Part A.

James L. German, a pioneer in early human genetic research turned 90

E. Passarge, 2016, American journal of medical genetics. Part A.

A DNA helicase in full Bloom

E. Passarge, 1995, Nature Genetics.

Further delineation of the Nijmegen breakage syndrome.

E. Seemanová, E. Passarge, R. Taalman, 1989, American journal of medical genetics.

Familial microcephaly with normal intelligence, immunodeficiency, and risk for lymphoreticular malignancies: a new autosomal recessive disorder.

J. Opitz, E. Seemanová, J. Houštěk, 1985, American journal of medical genetics.

Uniparental isodisomy for paternal 2p and maternal 2q in a phenotypically normal female with two isochromosomes, i(2p) and i(2q)

K. Zerres, T. Eggermann, B. Albrecht, 2001, Journal of medical genetics.

Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism

E. Blennow, S. Kitsiou‐Tzeli, A. Tsezou, 1998, European Journal of Human Genetics.

Everything the pediatrician ever wanted to know about HLA but was afraid to ask

E. Passarge, E. Valentine-Thon, 1980, European Journal of Pediatrics.

HLA‐A,B,C,DR typing and 17‐OHP determination for second trimester prenatal diagnosis of 21‐hydroxylase deficient CAH

E. Passarge, W. Sippell, F. Bidlingmaier, 1988, Prenatal diagnosis.

Three de novo losses and one insertion within a pericentric inversion of chromosome 6 in a patient with complete absence of expressive speech and reduced pain perception.

M. Poot, T. Haaf, E. Passarge, 2009, European journal of medical genetics.

Possible teratogenicity of trimethadione and paramethadione.

K. Ehlers, M. A. Engle, E. Passarge, 1970, Lancet.

Malformations of the central nervous system in trisomy 18 syndrome.

E. Passarge, W. Sueoka, C. True, 1966, The Journal of pediatrics.

Rapid diagnosis of maple syrup urine disease (branched chain ketoaciduria) by micro-enzyme assay in leukocytes and fibroblasts.

H. Rüdiger, E. Passarge, U. Langenbeck, 1973, Clinica chimica acta; international journal of clinical chemistry.

Mechanism of i(6p) formation in retinoblastoma tumor cells.

B. Horsthemke, E. Passarge, R. Becher, 1989, Cancer genetics and cytogenetics.

Two adults with Rubinstein–Taybi syndrome with mild mental retardation, glaucoma, normal growth and skull circumference, and camptodactyly of third fingers

R. Hennekam, D. Wieczorek, D. Peters, 2009, American journal of medical genetics. Part A.

Derivative chromosomal structures from a ring chromosome 4

E. Passarge, R. Niss, 1975, Human Genetics.

Microcephalic osteodysplastic primordial dwarfism type I/III in sibs.

E. Passarge, P. Meinecke, Eberhard Passarge, 1991, Journal of medical genetics.

Wither polygenic inheritance: Mapping Hirschsprung disease

E. Passarge, 1993, Nature Genetics.

Bloom's syndrome. VI. The disorder in Israel and an estimation of the gene frequency in the Ashkenazim.

Z. Laron, E. Passarge, J. German, 1977, American journal of human genetics.

Methods in Human Cytogenetics

U. Wolf, E. Passarge, H. G. Schwarzacher, 1974, Springer Berlin Heidelberg.

POTTER'S SYNDROME: CHROMOSOME ANALYSIS OF THREE CASES WITH POTTER'S SYNDROME OR RELATED SYNDROMES.

E. Passarge, J. Sutherland, 1965, American journal of diseases of children.

Prenatally detected trisomy 4 and 6 mosaicism—cytogenetic results and clinical phenotype

D. Wieczorek, W. Robinson, G. Gillessen‐kaesbach, 2003, Prenatal diagnosis.

Bloom's Syndrome. XII. Report from the Registry for 1987

E. Passarge, J. German, 1989, Clinical genetics.

Bloom's syndrome. V. Surveillance for cancer in affected families

E. Passarge, J. German, D. Bloom, 1977, Clinical genetics.

Association of ectrodactyly, ectodermal dysplasia, and cleft lip-palate.

E. Passarge, W. Haase, R. Rüdiger, 1970, American journal of diseases of children.

Bloom's Syndrome. VII. Progress report for 1978

E. Passarge, J. German, D. Bloom, 1979, Clinical genetics.

UV-light induced sister chromatid exchanges in xeroderma pigmentosum lymphocytes

A. Schönwald, E. Passarge, 1977, Human Genetics.

Bloom's Syndrome Registry

E. Passarge, J. German, 1990, International journal of dermatology.

Testicular Intratubular Bodies

A. J. Mcadams, E. Passarge, R. Bieger, 1965 .

AUTORADIOGRAPHY IN A BOY WITH XXY KARYOTYPE.

J. Thompson, E. Passarge, 1964, American journal of diseases of children.

Cooling velocity and cell recovery

H. Rüdiger, E. Passarge, W. Wöhler, 1975, Nature.

Functional deficiency of fibroblasts heterozygous for Bloom syndrome as specific manifestation of the primary defect.

C. Bartram, H. Rüdiger, E. Passarge, 1981, American journal of human genetics.

Rate of sister chromatid exchanges in Bloom syndrome fibroblasts reduced by co-cultivation with normal fibroblasts.

C. Bartram, H. Rüdiger, W. Harder, 1980, American journal of human genetics.

Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens

T. Dörk, D. Wieczorek, B. Dworniczak, 1997, Human Genetics.

Studies on the optimal cooling rate for freezing human diploid fibroblasts.

H. Rüdiger, E. Passarge, U. Wendel, 1973, Experimental cell research.

Toxicity of antibiotics on cultured human skin fibroblasts

H. Rüdiger, W. Byarugaba, E. Passarge, 1975, Humangenetik.

Frequency of sister chromatid exchanges in Bloom syndrome fibroblasts reduced by cocultivation with normal cells

C. Bartram, H. Rüdiger, E. Passarge, 1979, Human Genetics.

Chromatid exchanges in ataxia telangiectasia, Bloom syndrome, Werner syndrome, and xeroderrna pigmentosum

C. Bartram, E. Passarge, T. Koske-Westphal, 1976, Annals of human genetics.

Somatic recombination as possible prelude to malignant transformation.

C. Bartram, E. Passarge, 1976, Birth defects original article series.

Quinacrine mustard fluorescence of a second Y chromosome in a Y-autosomal translocation

E. Passarge, T. Koske-Westphal, Sabine Fründ, 2004, Humangenetik.

HLA-D and -DR antigens on human amniotic fluid cells. II. Heterogeneous expression of HLA-DR and other cell surface markers.

E. Passarge, H. Grosse-wilde, E. Valentine-Thon, 2008, Tissue antigens.

Congenital malformations in autosomal trisomy syndromes.

E. Passarge, J. Warkany, L. B. Smith, 1966, American journal of diseases of children.

Origins of human genetics. A personal perspective

E. Passarge, 2021, European Journal of Human Genetics.

Bibliography of Ulrich Wolf

C. Tyler-Smith, P. Yen, K. Hirschhorn, 2001, Cytogenetic and Genome Research.

Human chromosomal deficiency: The 4p- syndrome

E. Passarge, H. Altrogge, R. Rüdiger, 1970, Humangenetik.

Pachytene analysis in males heterozygous for a familial translocation (9;12;13) (q22; q22; q32) ascertained through a child with partial trisomy 9.

U. Löhrs, E. Passarge, R. Johannisson, 1988, Cytogenetics and cell genetics.

Syndrome of caudal regression in infants of diabetic mothers: observations of further cases.

E. Passarge, W. Lenz, 1966, Pediatrics.

CONGENITAL MALFORMATIONS AND MATERNAL DIABETES.

E. Passarge, 1965, Lancet.

Testicular feminisation and inguinal hernia.

J. Simpson, E. Passarge, J. German, 1973, Lancet.

Testicular intratubular bodies.

A. J. Mcadams, E. Passarge, R. Bieger, 1965, The Journal of clinical endocrinology and metabolism.

An excess of chromosome 1 breakpoints in male infertility

R. Stallings, C. Lundsteen, Z. Tümer, 2004, European Journal of Human Genetics.

Cerebro-hepato-renal syndrome. A newly recognized hereditary disorder of multiple congenital defects, including sudanophilic leukodystrophy, cirrhosis of the liver, and polycystic kidneys.

A. J. Mcadams, E. Passarge, 1967, The Journal of pediatrics.

X chromosome inactivation in X-linked hypohidrotic ectodermal dysplasia.

E. Passarge, E. Fries, 1973, Nature: New biology.

Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.

B. Lorenz, B. Horsthemke, D. Lohmann, 1997, American journal of human genetics.

The spectrum of RB1 germ-line mutations in hereditary retinoblastoma.

B. Horsthemke, D. Lohmann, E. Passarge, 1996, American journal of human genetics.

Color atlas of genetics

E. Passarge, Eberhard Passarge, 1995 .

Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma

B. Horsthemke, D. Lohmann, E. Passarge, 1994, Human Genetics.

Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs.

D. Wieczorek, H. Engels, E. Passarge, 1998, Journal of medical genetics.

A distinctive phenotype associated with an interstitial deletion 6q14 contained within a de novo pericentric inversion 6 (p11.2q15)

E. Passarge, 2001, Cytogenetic and Genome Research.

Heterozygote tests and genetic counseling in Maple Syrup Urine Disease

H. Rüdiger, E. Passarge, T. Grimm, 1975, Humangenetik.

Enhancement of amniotic fluid cell growth in culture

H. Rüdiger, E. Passarge, U. Wendel, 1974, Humangenetik.

Correction: Corrigendum: Transcriptional regulator PRDM12 is essential for human pain perception

Andreas C. Themistocleous, I. Katona, T. Wieland, 2015, Nature Genetics.

Severe developmental failure with coarse facial features, distal limb hypoplasia, thickened palmar creases, bifid uvula, and ureteral stenosis: a previously unidentified familial disorder with lethal outcome.

E. Passarge, D. Loose, W. Schmidt, 1971, The Journal of pediatrics.

Fetal manifestation of a chromosomal disorder: partial duplication of the long arm of chromosome 5 (5q33 to qter).

H. Rehder, E. Passarge, M. Bartsch-Sandhoff, 1982, Teratology.

[Robinow's fetal face-dwarfism syndrome].

E. Passarge, I. Wörner, R. Seel, 1974, Monatsschrift fur Kinderheilkunde.

Spectrum of small length germline mutations in the RB1 gene.

B. Horsthemke, D. Lohmann, E. Passarge, 1994, Human molecular genetics.

Improved prediction of complex diseases by common genetic markers: state of the art and further perspectives

Anne-Laure Boulesteix, Jens Brauer, Arndt Wilcke, 2016, Human Genetics.

[Diseases caused by genetic defects in lysosomal muco-polysaccharide-catabolism. Mucopolysaccharidoses].

H. Rüdiger, E. Passarge, U. Wendel, 1974, Deutsche medizinische Wochenschrift.

Trisomy 8 restricted to cultured fibroblasts.

E. Passarge, R. Niss, Eberhard Passarge, 1976, Journal of medical genetics.

Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma

B. Horsthemke, D. Lohmann, E. Passarge, 1994, Human Genetics.

Maternal origin of a de novo chromosome 8 deletion in a patient with Langer-Giedion syndrome

B. Horsthemke, E. Passarge, G. Senger, 1989, Human Genetics.

Syndrome of developmental retardation, facial and skeletal anomalies, and hyperphosphatasia in two sisters: nosology and genetics of the Coffin-Siris syndrome.

K. Zerres, E. Passarge, D. Emons, 1991, American journal of medical genetics.

No difference in expression of chromosomal fragile sites in patients with solid malignant tumours and normal controls

H. Rüdiger, E. Passarge, A. Schmidt, 1990, Genes, chromosomes & cancer.

The Human Genome and Disease

E. Passarge, 2003 .

Population cytogenetics, assignment of gene loci in autosomes, karyotype-phenotype correlations. A progress report on human cytogenetics.

E. Passarge, 1970, Humangenetik.

Identification of a frameshift mutation in the gene TWISTin a family affected with Robinow-Sorauf syndrome

G. Gillessen‐kaesbach, E. Passarge, J. Kunz, 1999, Journal of Medical Genetics.

Postaxial acrofacial dysostosis syndrome with microcephaly, seizures and profound mental retardation.

E. Passarge, H. Hauss-Albert, 1988, American journal of medical genetics.

PARAFFIN COMPRESS FOR HEAT THERAPY.

E. Passarge, J. Payne, B. A. Marklew, 1965, Lancet.

[Clinical, endocrinological, histological and chromosomal investigations on Klinefelter's syndrome].

E. Passarge, W. Bartsch, C. Schirren, 1979, Andrologia.

Human chromosomal deletion: two patients with the 4p- syndrome.

M. A. Engle, E. Passarge, J. German, 1970, The Journal of pediatrics.

The genetics of Hirschsprung's disease. Evidence for heterogeneous etiology and a study of sixty-three families.

E. Passarge, 1967, The New England journal of medicine.

Three brothers with mental and physical retardation, hydrocephalus, microcephaly, internal malformations, speech disorder, and facial anomalies: Mutchinick syndrome.

D. Wieczorek, W. Doerfler, B. Albrecht, 1997, American journal of medical genetics.

Girl with phenotypic abnormalities and a de novo, apparently balanced translocation 46,XX,t(5;10)(q35.2q11.2).

G. Gillessen‐kaesbach, E. Passarge, J. Wirth, 2001, American journal of medical genetics.

Molecular analysis of mutations in the gene FMR-1 segregating in fragile X families

I. Kennerknecht, M. Zank, E. Passarge, 1993, Human Genetics.

Encephalocele, polycystic kidneys, and polydactyly as an autosomal recessive trait simulating certain other disorders: the Meckel syndrome.

E. Passarge, S. Mecke, 1971, Annales de genetique.

Experience treating a patient with Bloom syndrome and acute myelogenous leukemia.

E. Passarge, B. Kremens, H. Grasemann, 1998, Medical and pediatric oncology.

HLA-D and -DR antigens on human amniotic fluid cells. I. Lack of expression of HLA-D.

E. Passarge, H. Grosse-wilde, E. Valentine-Thon, 2008, Tissue antigens.

Fc receptor blocking antibodies after active immunization for the treatment of recurrent spontaneous abortion.

R. Blasczyk, W. Luboldt, E. Passarge, 1991, Journal of reproductive immunology.

Application of linkage analysis to genetic counselling in families with hereditary retinoblastoma.

B. Horsthemke, E. Passarge, V. Greger, 1988, Journal of medical genetics.

Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locus

B. Horsthemke, E. Passarge, V. Greger, 1987, Human Genetics.

Construction of a chromosome 15-specific linking library and identification of potential gene sequences.

B. Horsthemke, E. Passarge, K. Buiting, 1988, Genomics.

Possible involvement of the retinoblastoma gene in undifferentiated sinonasal carcinoma

B. Horsthemke, E. Passarge, A. Bornemann, 1990, Cancer.

Anhidrotic ectodermal dysplasia as autosomal recessive trait in an inbred kindred

E. Passarge, C. T. Nuzum, W. Schubert, 2004, Humangenetik.

Autosomal recessive hypohidrotic ectodermal dysplasia with subclinical manifestation in the heterozygote.

E. Passarge, E. Fries, 1977, Birth defects original article series.

Spontaneous chromosomal instability

E. Passarge, 2004, Humangenetik.

Partial trisomy 13 presumably due to recombination in an inversion heterozygote and by unequal crossing‐over

E. Passarge, R. Niss, T. Koske-Westphal, 1978, Annals of human genetics.

Population cytogenetics assignment of gene loci to autosomes, karyotype-phenotype correlations

E. Passarge, 1970, Humangenetik.

Maple syrup urine disease: Rapid prenatal diagnosis by enzyme assay

H. Rüdiger, M. Mikkelsen, E. Passarge, 2004, Humangenetik.

Autoradiographic studies of human chromosomes

E. Passarge, J. German, J. Rock, 2004, Chromosoma.

3H-thymidine incorporation at the end of the S phase in cultured human lymphocytes

E. Passarge, D. Berghoff, 2004, Humangenetik.

Cornelia de Lange syndrome: evolution of the phenotype.

E. Passarge, H. Altrogge, S. Mecke, 1971, Pediatrics.

Prenatal diagnosis and management of congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

E. Passarge, 1988, Indian journal of pediatrics.

Analysis ofafamilial three waytranslocation involving chromosomes 3q,6q,and15qbyhigh resolution banding andfluorescent insitu hybridisation (FISH) showstwodifferent unbalanced karyotypes insibs

E. Passarge, R. Viersbach, B. Henke, 1998 .

Triosephosphate Isomerase Gene not Localized on the Short Arm of Chromosome 5 in Man

H. Rüdiger, G. Löhr, E. Passarge, 1970, Nature.

Benzpyrene induces sister chromatid exchanges in cultured human lymphocytes

C. Bartram, H. Rüdiger, E. Passarge, 1976, Nature.

Further patient with Angelman syndrome due to paternal disomy of chromosome 15 and a milder phenotype.

B. Horsthemke, B. Albrecht, G. Gillessen‐kaesbach, 1995, American journal of medical genetics.

Human chromosomal deletion: with the 4p-syndrome Two patients

E. Passarge, J. German, A. Engle, 1970 .

Epidermolysis bullosa hereditaria simplex. A kindred affected in 4 generations.

E. Passarge, 1965, The Journal of pediatrics.

Molecular analysis and predictive testing in retinoblastoma.

B. Horsthemke, D. Lohmann, E. Passarge, 1995, Ophthalmic genetics.

Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma.

B. Horsthemke, E. Passarge, V. Greger, 1991, American journal of medical genetics.

Use of the RB1 cDNA as a diagnostic probe in retinoblastoma families

B. Gallie, A. Goddard, B. Horsthemke, 1990, Clinical genetics.

EARLY DIAGNOSIS IN HEREDITARY RETINOBLASTOMA BY DETECTION OF MOLECULAR DELETIONS AT GENE LOCUS

B. Horsthemke, E. Passarge, V. Greger, 1987, The Lancet.

Deletion in one allele and a rare neutral DNA alteration in the other allele of the RB1 gene in a patient with bilateral retinoblastoma.

B. Horsthemke, B. Albrecht, E. Passarge, 1992, American journal of medical genetics.

A simple and nonradioactive method for detecting the Rb1.20 DNA polymorphism in the retinoblastoma gene.

D. Yandell, B. Horsthemke, E. Passarge, 1992, American journal of human genetics.

Microcephaly, seizures, genital hypoplasia, and abnormalities of the hands and feet in a 4‐year‐old boy with possible Wiedemann syndrome

D. Wieczorek, G. Gillessen‐kaesbach, E. Passarge, 1996, Clinical genetics.

New autosomal recessive lethal disorder with polycystic kidneys type Potter I, characteristic face, microcephaly, brachymelia, and congenital heart defects.

H. Rehder, B. Padberg, G. Gillessen‐kaesbach, 1993, American journal of medical genetics.

The early years of the ESHG leading to the reform of 1988 and the spirit of the Sestri Levante school

A. Chapelle, G. Romeo, E. Passarge, 2017, European Journal of Human Genetics.

Congenital osteogenesis imperfecta in three sibs

E. Passarge, S. Braga, 1981, Human Genetics.

Genetic counselling in cystic fibrosis

E. Passarge, U. Stephan, B. Eckerland, 1984, European Journal of Pediatrics.

[TGC Repeats in Intron 2 of the TCF4 Gene have a Good Predictive Power Regarding to Fuchs Endothelial Corneal Dystrophy].

E. Passarge, K. Hoffmann, E. Weidle, 2015, Klinische Monatsblatter fur Augenheilkunde.

Further characterization of the EAI factor induced by alloimmunization for treatment of recurrent abortion.

R. Blasczyk, W. Luboldt, E. Passarge, 1990, Immunology letters.

Application oflinkage analysis togenetic counselling infamilies withhereditary retinoblastoma

B. Horsthemke, E. Passarge, V. Greger, 1988 .

retinoblastoma . families with hereditary to genetic counselling in Application of linkage analysis

B. Horsthemke, E. Passarge, V. Greger, 2022 .

A nine-month-old boy with microcephaly, cataracts, intracerebral calcifications and dysmorphic signs: an additional observation of an autosomal recessive congenital infection-like syndrome?

D. Wieczorek, G. Gillessen‐kaesbach, E. Passarge, 1995, Genetic counseling.

The Chromosome Disorders: An Introduction for Clinicians

E. Passarge, 1970 .

Prenatal detection of a fetus hemizygous for the fragile X-chromosome

E. Seemanová, M. Macek, E. Passarge, 2004, Human Genetics.

Familial translocation (3?--;G?q+) and nondisjunction of chromosome in group G in two unrelated families.

E. Passarge, R. L. Shaw, S. W. Soikup, 1969, Cytogenetics.

Unilateral agenesis of the diaphragm

E. Passarge, J. German, H. Halsey, 2004, Humangenetik.

Possible genetic heterogeneity of X-linked ichthyosis.

B. Post, E. Passarge, E. Schöpf, 1971, Birth defects original article series.

Differential expression of fragile site Xq27 in cultured fibroblasts from hemizygotes and heterozygotes and its implications for prenatal diagnosis.

E. Passarge, A. Schmidt, 1986, American journal of medical genetics.

Improved prediction of complex diseases by common genetic markers: state of the art and further perspectives

A. Boulesteix, H. Kirsten, J. Brauer, 2016, Human Genetics.

Genetic heterogeneity of XY gonadal dysgenesis (Swyer syndrome): H-Y antigen-negative XY gonadal dysgenesis associated with inflammatory bowel disease.

U. Wolf, E. Passarge, 1981, American journal of medical genetics.

Identiﬁcation of a frameshift mutation in

E. Passarge, J. Kunz, B. Fritz, 1999 .

[Gastroinstestinal hemorrhage in Turner's syndrome due to telangiectasias in the intestinal wall].

E. Passarge, 1968, Deutsche medizinische Wochenschrift.

The delivery of genetic counseling services in Europe

I. Emerit, F. Vogel, A. Czeizel, 2004, Human Genetics.

Bloom's syndrome XI. Progress report for 1983

E. Passarge, J. German, D. Bloom, 1984, Clinical genetics.

Familial occurrence of a short rib syndrome with hydrops fetalis but without polydactyly.

E. Passarge, 1983, American journal of medical genetics.

Familial translocation (3?--;G?- q+) and nondisjunction of chromosome in group G in two unrelated families.

E. Passarge, D. Becroft, S. Soukup, 1969, Cytogenetics.

Reply to Dr. Taybi

E. Passarge, P. Meinecke, 1992 .

The Xg blood group and genetics.

E. Passarge, 1966, American journal of diseases of children.

In Memoriam: “Holstein cows in Holstein.” Victor A. McKusick: 40 years of remembrance from Europe

E. Passarge, 2021, American journal of medical genetics. Part A.

Thalidomid-Embryopathie 60 Jahre

E. Passarge, 2022, DMW - Deutsche Medizinische Wochenschrift.

Frequency of sister chromatid exchanges in Bloom syndrome fibroblasts reduced by cocultivation with normal cells

C. Bartram, H. Rüdiger, E. Passarge, 1979, Human Genetics.

Alpha1-antitrypsin phenotypes in sex chromosome mosaicism.

E. Passarge, F. Kueppers, H. Rudiger, 1975, Journal of medical genetics.

GENETIC DISORDERS IN GYPSIES

E. Passarge, 1975, The Lancet.