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European Journal of Pediatrics|June 13, 1998
Congenital hydrocephalus: nosology and guidelines for clinical approach and genetic counsellingC Schrander-Stumpel, J P FrynsGenetic Counseling (Geneva, Switzerland)|May 23, 2007
Kabuki syndrome: description of a 2-year old Roumanian boy and review of the literatureD M Ioan, J P FrynsJournal of Pediatric Ophthalmology and Strabismus|October 28, 2005
Unilateral Peters' anomaly in a patient with DiGeorge syndromeI Casteels, K DevriendtClinical Genetics|October 30, 2009
Novel PORCN mutations in focal dermal hypoplasiaG Froyen, K Govaerts, H Van Esch, et al.American Journal of Human Genetics|March 26, 1999
Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1K Devriendt, G Matthijs, R Van Dael, et al.Annales De Genetique|January 1, 1979
Possible excess of mental handicap and congenital malformations in autosomal reciprocal translocationsJ P Fryns, H van den BergheAmerican Journal of Medical Genetics|January 1, 1988
Acrofacial dysostosis with postaxial limb deficiencyJ P Fryns, H Van den BergheClinical Genetics|October 1, 1986
An asymmetric type of chondrodysplasia in an adult male. Another example of postzygotic mutation for an autosomal dominant gene?J P Fryns, H van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1997
On the nosology of the craniodigital syndromes: report of a family and review of the literatureD Soekarman, P Volcke, J P FrynsPageof 90