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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.Revue Belge De Medecine Dentaire|January 1, 1992
[Survey on HIV and the control of infection]F Prieels, P De CockGenetic 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 DevriendtBiology of the Neonate|January 7, 2004
Information processing in very-low-birth-weight children with and without attention deficit disorderS T Potgieter, P de CockJournal 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 ButtiensPageof 90