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Clinical Genetics|December 1, 1985
Mosaic tetrasomy 12pS Gilgenkrantz, P Droulle, M Schweitzer, et al.Genomics|June 10, 1995
A high-resolution interval map of the q21 region of the human X chromosomeC Philippe, C Arnould, F Sloan, et al.Annales De Genetique|January 1, 1992
Incontinentia pigmenti (type 1) and X;5 translocationP Bitoun, C Philippe, M Cherif, et al.Oncogene|July 1, 1990
Sublocalisation of the X breakpoint in the translocation (X; 18)(p11.2; q11.2) primary change in synovial sarcomasS Gilgenkrantz, M Chery, M Teboul, et al.Human Genetics|October 1, 1990
Distal trisomy 14q. I. Clinical and cytogenetical studiesS Gilgenkrantz, J Vigneron, M O Peter, et al.Human Genetics|November 1, 1990
A 45,X male with molecular evidence of a translocation of Y euchromatin onto chromosome 1N Abbas, G Novelli, N C Stella, et al.Journal De Genetique Humaine|May 1, 1987
[True hermaphroditism and double fertilization]S GilgenkrantzBulletin De L'Association Des Anatomistes|December 1, 1987
[A collaborative study of habitual abortion in couples with normal and abnormal karyotypes]S GilgenkrantzLa Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|February 23, 1977
[The present role of genetic counseling]S GilgenkrantzHuman Genetics|September 1, 1992
Linkage study in a large pedigree with Stickler syndrome: exclusion of COL2A1 as the mutant geneJ Bonaventure, C Philippe, G Plessis, et al.Pageof 24