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Journal of Medical Genetics|May 1, 1997
Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndromeK Devriendt, P Petit, G Matthijs, et al.Clinical Genetics|June 11, 1999
Partial DiGeorge syndrome in two patients with a 10p rearrangementH Van Esch, P Groenen, S Daw, et al.Cytogenetics and Cell Genetics|January 1, 1996
Isolation of cosmids corresponding to the chromosome breakpoints of a de novo autosomal translocation, t(6;19)(p21;q13.1), in a patient with multicystic renal dysplasiaP M Groenen, E Garcia, R Thoelen, et al.Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Parenting, family contexts, and personality characteristics in youngsters with VCFSP Prinzie, A Swillen, B Maes, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|September 15, 2000
Genetic control of intra-uterine growthK DevriendtJournal of Medical Genetics|July 9, 2009
Distal limb deficiencies, micrognathia syndrome, and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangementsB I Dimitrov, T de Ravel, J Van Driessche, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Corpus callosum agenesis in Coffin-Lowry syndromeD Soekarman, J P FrynsGenetic Counseling (Geneva, Switzerland)|February 1, 2003
The Prader-Willi syndrome and the Angelman syndromeA Vogels, J P FrynsAmerican Journal of Medical Genetics|October 1, 1987
X-linked mental retardation with marfanoid habitusJ P Fryns, M ButtiensGenetic Counseling (Geneva, Switzerland)|January 1, 1994
Normal/trisomy 13 mosaicism in a 38-year-old maleP Petit, J P FrynsPageof 105