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Human Genetics|February 15, 1979
Partial trisomy 18q12, due to intrachromosomal duplication, is not associated with typical 18 trisomy phenotypeJ P Fryns, L Vinken, J Marien, et al.Human Genetics|March 12, 1979
Partial duplication of the short arm of chromosome 10. Karyotype: 46,XX,dup(10p)(pter to p12::p12::p12 to qter)J P Fryns, J Deroover, J Haegeman, et al.Journal De Genetique Humaine|June 1, 1983
[Body and craniofacial biometric study of 26 Klinefelter patients compared to 307 controls]A Gueguen, A Tumba, H van den Berghe, et al.Clinical Genetics|September 1, 1983
Germinal mosaicism in achondroplasia: a family with 3 affected siblings of normal parentsJ P Fryns, A Kleczkowska, H Verresen, et al.Acta Paediatrica Scandinavica|September 1, 1983
Congenital bowing of the long bones. An example of a campomelic syndrome of the short-limbed normocephalic subtypeJ P Fryns, P Annicq, M Ulrix, et al.Clinical Genetics|October 1, 1996
The Floating-Harbor syndrome: two affected siblings in a familyJ P Fryns, A Kleczkowska, J Timmermans, et al.Human Genetics|October 14, 1977
Partial monosomy of the long arm of chromosome 16 in a malformed newborn: karyotype 46,XX,del(16))q21)J P Fryns, S Melchoir, J Jaeken, et al.American Journal of Medical Genetics|August 9, 1996
New findings in the behavioral profile of young FraX femalesM Borghgraef, S Umans, J Steyaert, et al.Clinical Genetics|July 1, 1996
On two patients with and without the classical Wolf-Hirschhorn syndrome (WHS) sharing the same chromosome 4p16.3 specific probe deletion: evidence of a contiguous gene deletion syndromeP Petit, J Schmit, H Van den Berghe, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Increased head circumference and facial cleft as presenting signs of the nevoid basal-cell carcinoma syndromeD Soekarman, J P Fryns, P Casaer, et al.Pageof 89