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Annales De Genetique|January 1, 1988
Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndromeI Henry, M Jeanpierre, F Barichard, et al.Human Genetics|January 1, 1987
Partial androgen receptor deficiency and mixed gonadal dysgenesis in Drash syndromeC Turleau, P Niaudet, C Sultan, et al.Human Genetics|May 1, 1988
Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11M Andersson, D C Page, D Pettay, et al.Cancer Genetics and Cytogenetics|April 15, 1985
Cytogenetic forms of retinoblastoma: their incidence in a survey of 66 patientsC Turleau, J de Grouchy, F Chavin-Colin, et al.American Journal of Medical Genetics|March 1, 1989
Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomaliesC Turleau, M O Cabanis, D Girault, et al.Annales De Genetique|January 1, 1987
The beta amyloid protein (AD-AP) cDNA hybridizes in normal and Alzheimer individuals near the interface of 21q21 and q22.1V Blanquet, D Goldgaber, C Turleau, et al.Humangenetik|September 23, 1975
Partial trisomy 9q: a new syndromeC Turleau, J de Grouchy, F Chavin-Colin, et al.Annales De Genetique|January 1, 1987
From oocyte to embryo: a model, deduced from in vitro fertilization, for natural selection against chromosome abnormalitiesM Plachot, J de Grouchy, A M Junca, et al.Cancer Genetics and Cytogenetics|August 1, 1982
Retinoblastoma, deletion 13q14, and esterase D: application of gene dosage effect to prenatal diagnosisC Junien, S Despoisse, C Turleau, et al.Human Genetics|August 1, 1987
Maternal origin of a de novo balanced t(21q21q) identified by ets-2 polymorphismN Créau-Goldberg, A Gegonne, J Delabar, et al.Pageof 13