L’AGE MATERNEL ET LE RANG DE NAISSANCE DANS UN ECHANTILLON DE JUMEAUX von Lamy, Maurice, Frézal, Jean, De Grouchy, Jean, Chryssostomidou, Melle

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Chromosome phylogenies of man, great apes, and old world monkeys von DE GROUCHY, J

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Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases von TURLEAU, C, DE GROUCHY, J, CHAVIN-COLIN, F, MARTELLI, H, VOYER, M, CHARLAS, R

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Incontinentia pigmenti and X-autosome translocations: non-isotopic in situ hybridization with an X-centromere-specific probe (pSV2X5) reveals a possible X-centromeric breakpoint in... von CROLLA, J. A, GILGENKRANTZ, S, DE GROUCHY, J, KAJII, T, BOBROW, M

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Maternal origin of a de novo balanced t(21q21q) identified by ets-2 polymorphism von CREAU-GOLDBERG, N, GEGONNE, A, DELABAR, J, COCHET, C, CABANIS, M.-O, STEHELIN, D, TURLEAU, C, DE GROUCHY, J

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Chromosomal Phylogeny of the Primates von Grouchy, J, Turleau, C, Finaz, C

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New gene assignments in the rabbit (Oryctolagus cuniculus). Comparison with other species von Soulié, J, de Grouchy, J

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DNA polymorphism analysis in families with recurrence of free trisomy 21 von Pangalos, Constantinos G, Talbot Jr., Conover C, Lewis, John G, Adelsberger, Patricia A, Petersen, Michael B, Serre, Jean-Louis, Rethoré, Marie-Odile, de Blois, Marie-Christine, Parent, Philipe, Schinzel, Albert A, Binkert, Franz, Boue, Joelle, Corbin, Elisabeth, Croquette, M F, Gilgenkrantz, Simone, de Grouchy, Jean, Bertheas, M F, Prieur, Marguerite, Raoul, Odile, Serville, Framcoise, Siffroi, J P, Thepot, Francois, Lejeune, Jerome, Antonarakis, Stylianos E

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Identification of individual chromosomes in the human karyotype by their banding pattern after proteolytic digestion von Finaz, Catherine, Grouchy, Jean

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CHROMOSOMES IN MALIGNANT LYMPHOMAS von Lejeune, Jérôme, de Grouchy, Jean

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Multibranched chromosomes in the ICF syndrome: Immunodeficiency, centromeric instability, and facial anomalies von Turleau, Catherine, Cabanis, Marie-Odile, Girault, Danièle, Ledeist, Françoise, Mettey, René, Puissant, Hugues, Prieur, Marguerite, De Grouchy, Jean

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Chromosome 18: A topologic approach von de Grouchy, Jean

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Partial androgen receptor deficiency and mixed gonadal dysgenesis in Drash syndrome von TURLEAU, C, NIAUDET, P, SULTAN, C, RAULT, G, ABDELMOUTALEB MAHFOUD, NIHOUL-FEKETE, C, IRIS, L, DE GROUCHY, J

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Conservation of the human COL1A1-TK-GAA synteny and homoeologous assignment in the African green monkey and the baboon (Cercopithecoidae) von CREAU-GOLDBERG, N, TURLEAU, C, COCHET, C, HUERRE, C, JUNIEN, C, DE GROUCHY, J

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L'homme et l'hérédité von J., A., Lamy, Maurice, de Grouchy, Jean

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A Genetic Study of β-Aminoisobutyric Acid Excretion1 von De Grouchy, Jean, Sutton, H. Eldon

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Rett phenotype with X/autosome translocation: Possible mapping to the short arm of chromosome X von Journal, Hubert, Melki, Judith, Turleau, Catherine, Munnich, Arnold, de Grouchy, Jean

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Genetic and non-genetic factors in the etiology of congenital heart disease: a study of 1188 cases von LAMY, M, DE GROUCHY, J, SCHWEISGUTH, O

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CHROMOSOME STUDIES IN LEUKÆMIA von Baikie, A.G., Court Brown, W.M., Jacobs, PatriciaA, Grouchy, JeanDe

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Retinoblastoma, deletion 13q14, and esterase D: Application of gene dosage effect to prenatal diagnosis von Junien, Claudine, Despoisse, Suzy, Turleau, Catherine, Nicolas, Henriette, Picard, François, Le Marec, Bernard, Kaplan, Jean-Claude, de Grouchy, Jean

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