J. de Grouchy

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Catalase determination in various etiologic forms of Wilms' tumor and gonadoblastoma.

C. Junien, G. Lenoir, M. Rethoré, 1983, Cancer genetics and cytogenetics.

[Identity of karyotypes of Papio papio and Macaca mulatta in R, G, C banding and Ag-NOR].

J. de Grouchy, C. Cochet, C. Finaz, 1978, Annales de genetique.

Chromosome analysis of human oocytes and embryos: does delayed fertilization increase chromosome imbalance?

J. Mandelbaum, J. Cohen, J. de Grouchy, 1988, Human reproduction.

Constitutional karyotypes in retinoblastoma.

C. Turleau, J. de Grouchy, 1987, Ophthalmic paediatrics and genetics.

Dermatoglyphic patterns in senile dementia of Alzheimer's type.

Y. Lamour, J. de Grouchy, M. Roudier, 1988, Annales de genetique.

[Chromosomal phylogeny of man and the anthropomorphic primates. (Pan troglodytes, Gorilla gorilla, Pongo pygmaeus). Attempt at reconstitution of the karyotype of the common ancestor].

C. Turleau, J. de Grouchy, M. Klein, 1972, Annales de genetique.

[Pericentric inversion of no. 3, homozygous and heterozygous, and centromeric transposition of no. 12 in a family of orangutans. Implications for evolution].

C. Turleau, J. de Grouchy, C. Chavin-Colin, 1975, Annales de genetique.

[The price of life].

J. de Grouchy, 1976, Archives francaises de pediatrie.

Models for clonal evolutions: a study of chronic myelogenous leukemia.

J. Cantú, J. de Grouchy, J. Bousser, 1966, American journal of human genetics.

Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies.

F. Ledeist, M. Cabanis, M. Prieur, 1989, American journal of medical genetics.

Are clinical and biological IVF parameters correlated with chromosomal disorders in early life: a multicentric study.

A. Veiga, J. Mandelbaum, G. Calderón, 1988, Human reproduction.

[A case of 46 XX gonadoblastoma].

J. de Grouchy, C. Pélissier, H. Yaneva, 1970, Annales d'endocrinologie.

Gonadoblastoma in gonadal dysgenesis: a report of two cases with 46,XY-45,X mosaicism.

F. Dray, J. de Grouchy, R. Rappaport, 1969, The Journal of pediatrics.

Assignment of phosphoglycerate mutase (PGAMA) to human chromosome 10. Regional mapping of GOT1 and PGAMA to subbands 10q26.1 (or q25.3).

C. Junien, C. Turleau, R. Fundele, 1982, Annales de genetique.

[Satellited Y chromosome (Yqs) and nucleolar organizer occurring de novo].

C. Turleau, J. de Grouchy, F. Chavin-Colin, 1978, Annales de genetique.

XO-XY-Xy mosaicism and Turner's syndrome in an 18-year-old girl.

I. Emerit, J. de Grouchy, P. Corone, 1966, Annales de genetique.

TRUE HERMAPHRODITISM WITH XX-XY MOSAICISM, PROBABLY DUE TO DOUBLE FERTILIZATION OF THE OVUM.

J. Frézal, M. Lamy, M. Jayle, 1965, The Journal of clinical endocrinology and metabolism.

Mixed gonadal dysgenesis. Two additional pediatric cases.

J. Frézal, M. Lamy, J. de Grouchy, 1966, American journal of diseases of children.

Lymphocyte activation in allograft recipients.

J. de Grouchy, M. Lacombe, J. Hamburger, 1972, Transplantation proceedings.

Aneusomie de recombinaison: three further examples.

J. de Grouchy, M. Lamy, M. Aussannaire, 1966, American journal of human genetics.

[FAMILIAL AND ANEUPLOID MARKER CHROMOSOMES. POSSIBLE ROLE OF CHROMOSOME INTERACTION].

M. Lamy, J. de Grouchy, S. Thieffry, 1964, Annales de genetique.

PURE GONADAL DYSGENESIS; REPORT OF A CASE.

J. de Grouchy, C. Nezelof, N. Josso, 1965, American journal of diseases of children.

Cytogenetic analysis and developmental capacity of normal and abnormal embryos after IVF.

J. Mandelbaum, J. Cohen, J. de Grouchy, 1989, Human reproduction.

CHROMOSOMAL AUTORADIOGRAPHY IN THE CRI DU CHAT SYNDROME.

J. Lejeune, J. German, J. de Grouchy, 1964, Cytogenetics.

[Chromosomal breakage in incontinentia pigmenti. Study of a family].

J. de Grouchy, P. Bégin, J. Bonnette, 1972, Annales de genetique.

Genetic diseases, chromosome rearrangements, and malignancy.

J. de Grouchy, 1966, Annals of internal medicine.

From oocyte to embryo: a model, deduced from in vitro fertilization, for natural selection against chromosome abnormalities.

J. Mandelbaum, C. Turleau, J. Cohen, 1988, Annales de genetique.

[Trisomy 10 p. A previously reported case explained by binding].

C. Turleau, J. de Grouchy, M. Doussau de Bazignan, 1976, Annales de genetique.

[Trisomy 9p : 2 further cases].

C. Turleau, J. de Grouchy, F. Chavin-Colin, 1974, Annales de genetique.

Comparison of banding patterns of human chromosomes obtained with heating, fluorescence, and proteolytic digestion.

B. Dutrillaux, J. Lejeune, J. de Grouchy, 1972, Cytogenetics.

Embryonic testicular regression syndrome and severe mental retardation in sibs.

A. Gompel, C. Turleau, M. le Merrer, 1985, Annales de genetique.

Chromosome investigations in early life. II. Human preimplantation embryos.

J. Mandelbaum, J. Cohen, J. de Grouchy, 1987, Human reproduction.

[Partial trisomy C by t(Cq-; Dp+) translocation with a C(p- q+) remnant].

J. Aicardi, J. Chevrie, J. de Grouchy, 1967, Archives francaises de pediatrie.

[Sex linked mental deficiency, unusual facies, macroorchidism and fragile site on chromosome X (author's transl)].

P. Czernichow, C. Turleau, J. de Grouchy, 1979, Annales de genetique.

White blood cell transfusions.

G. Mathé, L. Schwarzenberg, J. de Grouchy, 1965, Israel journal of medical sciences.

Beta amyloid gene duplication in Alzheimer's disease and karyotypically normal Down syndrome

J. Delabar, D. Goldgaber, Y. Lamour, 1987, Science.

Chromosomal phylogeny of the primates.

C. Turleau, J. de Grouchy, C. Finaz, 1978, Annual review of genetics.

Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complex.

C. Junien, R. Tenconi, J. Dufier, 1980, Annales de genetique.

[Mosaic trisomy 14 due to an iso dicentric chromosome (author's transl)].

C. Turleau, A. Cornu, J. de Grouchy, 1980, Annales de genetique.

[Distal 14q trisomy].

C. Turleau, J. de Grouchy, F. Chavin-Colin, 1983, Annales de genetique.

Beckwith-Wiedemann syndrome. Clinical comparison between patients with and without 11p15 trisomy.

C. Turleau, J. de Grouchy, 1985, Annales de genetique.

[Intercalary deletions of 9q].

C. Turleau, J. de Grouchy, J. Chabrolle, 1978, Annales de genetique.

Chromosomal Abnormalities and Congenital Heart Disease

I. Emerit, P. Vernant, J. de Grouchy, 1967, Circulation.

Assignment of the ABO-Np-AK1 linkage group to chromosome 9 in man-hamster hybrids.

D. Weil, J. Frézal, J. de Grouchy, 1976, Cytogenetics and cell genetics.

[Distal trisomy 15q].

C. Turleau, J. de Grouchy, F. Chavin-Colin, 1977, Annales de genetique.

Genetic and non-genetic factors in the etiology of congenital heart disease: a study of 1188 cases.

M. Lamy, J. de Grouchy, O. Schweisguth, 1957, American journal of human genetics.

A cytogenetic survey of 110 baboons (Papio cynocephalus).

J. de Grouchy, J. Soulié, 1981, American journal of physical anthropology.

[6-12 13-15 translocation and partial 6-12 trisomy (probably 10)].

J. de Grouchy, J. Canet, 1965, Annales de Genetique.

[COMPLEX MALFORMATIONS OF THE UPPER LIMBS ASSOCIATED WITH CONGENITAL HEART DISEASE. APROPOS OF 6 CASES].

I. Emerit, P. Vernant, M. Laval-Jeantet, 1965, Acta geneticae medicae et gemellologiae.

[PARTIAL DELETION OF THE LONG ARMS OF THE CHROMOSOME 18].

M. Lamy, J. de Grouchy, P. Royer, 1964, Pathologie et biologie.

Cytogenetic forms of retinoblastoma: their incidence in a survey of 66 patients.

C. Junien, A. Leblanc, C. Turleau, 1985, Cancer genetics and cytogenetics.

Retinoblastoma, deletion 13q14, and esterase D: application of gene dosage effect to prenatal diagnosis.

C. Junien, C. Turleau, S. Despoisse, 1982, Cancer genetics and cytogenetics.

Chromosomal breakage in diffuse scleroderma. A study of 27 patients.

I. Emerit, J. de Grouchy, J. Camus, 1971, Revue europeenne d'etudes cliniques et biologiques. European journal of clinical and biological research.

Chromosome investigations in early life. I. Human oocytes recovered in an IVF programme.

J. Mandelbaum, J. Cohen, J. de Grouchy, 1986, Human reproduction.

[DUPLICATION OF A PH CHROMOSOME AND SUGGESTION OF CLONAL EVOLUTION IN CHRONIC MYELOCYTIC LEUKEMIA IN ACUTE TRANSFORMATION].

J. de Grouchy, G. Bilski‐Pasquier, C. D. de Nava, 1965, Nouvelle revue francaise d'hematologie.

Physical map around the retinoblastoma gene: possible genomic imprinting suggested by NruI digestion.

V. Blanquet, C. Turleau, J. de Grouchy, 1991, Genomics.

[The heart in Turner-Ullrich syndrome. (Study of 26 personal cases and review of cases comprising a chromosomal study)].

I. Emerit, P. Vernant, J. de Grouchy, 1966, Archives des maladies du coeur et des vaisseaux.

[Cytogenetic, biochemical and morphological studies of a continuous cell line (Cy-LMC-1)].

M. Paintrand, J. de Grouchy, J. Marchand, 1970, Annales de Genetique.

[Fibroblasts in culture during mucopolysaccharidoses: the effect of serum on metachromasy].

P. Maroteaux, J. de Grouchy, M. Hors-Cayla, 1968, Annales de genetique.

Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndrome.

J. Mallet, C. Junien, C. Turleau, 1988, Annales de genetique.

[Pure trisomy 9p 47,XX,+ del(9) (q11). Discovery of one cell 46,XX, del(9) (q11) in the father].

C. Turleau, J. de Grouchy, F. Chavin-Colin, 1975, Annales de genetique.

Fifty-million-year evolution of chromosome 1 in the primates. Evidence from banding and gene mapping.

J. Frézal, J. de Grouchy, C. Cochet, 1977, Cytogenetics and cell genetics.

Two patients with interstitial del (14q), one with features of Holt-Oram syndrome. Exclusion mapping of PI (alpha-1-antitrypsin).

M. Dautzenberg, C. Turleau, J. de Grouchy, 1984, Annales de genetique.

[Study by fluorescence of a trisomy C mosaic, probably 8: 46,XY-47,XY,?8+].

C. Turleau, J. de Grouchy, C. Léonard, 1971, Annales de genetique.

[Interstitial deletion in the long arm of chromosome 7].

C Turleau, M. Cabanis, C. Turleau, 1988, Annales de genetique.

[A new observation of chromosome aberrations 18p].

J. de Grouchy, A. Rossier, N. Joab, 1967, Annales de Genetique.

[Partial trisomy for the long arm of a C chromosome (?6) through t(Gp+;Cqs+) translocation].

J. Aicardi, I. Emerit, J. de Grouchy, 1969, Annales de Genetique.

[Turner syndrome 45,X-46,XXq+].

I. Emerit, J. de Grouchy, A. Dubreuil, 1970, Annales d'Endocrinologie.

Mapping of the gene for glutathione reductase on chromosome 8.

A. de la Chapelle, C. Turleau, P. Aula, 1976, Annales de genetique.

[Ring of the chromosome 4. II. Without facial dysmorphism].

J. Limal, C. Turleau, J. de Grouchy, 1977, Annales de Genetique.

The beta amyloid protein (AD-AP) cDNA hybridizes in normal and Alzheimer individuals near the interface of 21q21 and q22.1.

J. Delabar, D. Goldgaber, V. Blanquet, 1987, Annales de genetique.

[46, XX, 1q-, 2q-, Dq+, 16q+ karyotype in a polymalformed child].

J. de Grouchy, F. Lautmann, 1968, Annales de genetique.

[Gene localization in the chimpanzee (Pan troglodytes). Comparison with the factor mapping of man (Homo sapiens)].

J. Frézal, J. de Grouchy, C. Cochet, 1975, Annales de genetique.

[The felidae: chromosomal evolution].

J. de Grouchy, M. Klein, M. Roubin, 1973, Annales de genetique.

[Karyotypic evolution in man and chimpanzees. A comparative study of band topographies after controlled denaturation].

C. Turleau, J. de Grouchy, M. Klein, 1972, Annales de genetique.

Confirmation of the regional assignment of peptidase A (PEPA) to 18q23 by gene dosage studies.

C. Junien, C. Turleau, J. de Grouchy, 1980, Annales de genetique.

A case of?6p- chromosomal aberration.

J. Veslot, J. de Grouchy, J. Bonnette, 1968, American journal of diseases of children.

[46,XX/46,XX,del (10) (p13)/47,XX,+r/47,XX,del (10) (p13), + r mosaicism and partial trisomy 10p phenotype (author's transl)].

C. Junien, J. Lejeune, M. Rethoré, 1979, Annales de genetique.

Incontinentia pigmenti (IP) and r(X). Tentative mapping of the IP locus to the X juxtacentromeric region.

C. Turleau, P. Maroteaux, J. de Grouchy, 1985, Annales de genetique.

[17-18 RING-CHROMOSOMES AND CONGENITAL MALFORMATIONS IN A YOUNG GIRL].

M. Lamy, J. de Grouchy, J. Marie, 1964, Annales de genetique.

Two cases of del(13q)-retinoblastoma and two cases of partial trisomy due to a familial insertion.

A. Leblanc, C. Turleau, J. de Grouchy, 1983, Annales de genetique.

[Heterozygosity and homozygosity for a pericentric inversion of human chromosone 3].

C. Turleau, J. de Grouchy, A. Betz, 1974, Annales de genetique.

Osteoarticular abnormalities and orthopedic complications in children with chromosomal aberrations.

J. Pouliquen, J. de Grouchy, G. Finidori, 1983, Annales de genetique.

["True" microcephaly with dominant-inheritance chorioretinal dysplasia].

J. Aicardi, J. Dufier, J. de Grouchy, 1980, Annales de Genetique.

Panel of twenty-five independent man-rodent hybrids for human genetic marker mapping.

M. Gross, D. Weil, J. Frézal, 1986, Annales de genetique.

[STUDY OF A PAIR OF MONOZYGOTIC TWINS ONE OF WHOM WAS AFFLICTED WITH MYOPATHY (PSEUDO-HYPERTROPHIC FORM)].

J. Frézal, M. Lamy, J. de Grouchy, 1963, Acta geneticae medicae et gemellologiae.

[Excess of males in trisomy 21 (author's transl)].

A. Bernheim, J. de Grouchy, C. Chastang, 1979, Annales de genetique.

A chromosomal theory of carcinogenesis.

J. de Grouchy, C. D. de Nava, 1968, Annals of internal medicine.

Cytogenetic investigation in 413 couples with spontaneous abortions.

C. Turleau, J. de Grouchy, J. Grouchy, 1979, European journal of obstetrics, gynecology, and reproductive biology.

Comparative gene mapping of man and Cebus capucinus: a study of 23 enzymatic markers.

C. Turleau, J. de Grouchy, C. Cochet, 1981, Cytogenetics and cell genetics.

[Fetomaternal transfusion of blood lymphocytes and identification of the sex of the fetus].

J. de Grouchy, C. Trébuchet, 1971, Annales de Genetique.

[2 familial translocations occurring together in each of 2 sisters, one balanced, the other partial trisomic 10q].

J. de Grouchy, C. Finaz, J. Roy, 1972, Annales de genetique.

Molecular detection of constitutional deletions in patients with retinoblastoma.

V. Blanquet, C. Turleau, J. de Grouchy, 1991, American journal of medical genetics.

NM1 keratinocytes display biochemical markers of keratinization.

J. de Grouchy, J. Thivolet, M. Faure, 1989, The Journal of investigative dermatology.

[Cytogenetic study of 3 cases of multiple cutaneous leiomyomatosis].

C. Turleau, J. de Grouchy, P. Venencie, 1988, Annales de dermatologie et de vénéréologie.

New gene assignments in the baboon and new chromosome homoeologies with man.

C. Turleau, J. de Grouchy, C. Cochet, 1983, Annales de Genetique.

Comparative gene mapping of the baboon (Papio papio) and man.

C. Turleau, J. de Grouchy, C. Cochet, 1982, Annales de Genetique.

Gene mapping of Microcebus murinus (Lemuridae): a comparison with man and Cebus capucinus (Cebidae).

C. Turleau, J. de Grouchy, C. Cochet, 1982, Cytogenetics and cell genetics.

Mapping around the Xq13.1 breakpoints of two X/A translocations in hypohidrotic ectodermal dysplasia (EDA) female patients.

B. Plougastel, E. Bakker, V. Blanquet, 1992, Genomics.

[Trisomy 13qter by tandem duplication 46, XX, dir dup 13 (q21 qter), 9qh+].

C. Turleau, J. de Grouchy, M. Briard, 1978, Annales de Genetique.

[The chromosome anomaly of Waldenström's disease].

J. de Grouchy, A. Broustet, G. Catanzano, 1965, Annales de genetique.

[PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME 5. INDIVIDUALIZATION OF A NEW MORBID STATE].

J. Lejeune, M. Gautier, R. Turpin, 1964, La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris.

Hemophilia A in a phenotypic female with normal male karyotype associated with a low factor XII level.

J. de Grouchy, B. Andréassian, D. Ménaché, 1980, Annales de genetique.

[Ph-1 chromosome and loss of small acrocentrics in a chronic myeloid leukemia of prolonged development in a man].

J. de Grouchy, J. Bousser, G. Bilski‐Pasquier, 1966, Annales de Genetique.

[Chromosome analyses in idiopathic acquired sideroblastic anemia. A study of 6 cases].

R. Zittoun, J. de Grouchy, J. Bousser, 1966, Nouvelle revue francaise d'hematologie.

[The price of life].

J. de Grouchy, 1976, Archives francaises de pediatrie.