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Annales De Genetique|January 1, 1994
Lens dislocation and optic nerve hypoplasia in ring chromosome 21 mosaicismF M Meire, J P FrynsGenetic Counseling (Geneva, Switzerland)|February 26, 2009
Unilateral radio-ulnar synostosis and idic-Y chromosomeL De Smet, J P FrynsAmerican Journal of Medical Genetics|October 16, 1996
Retinitis pigmentosa in a young man with Noonan syndrome: further evidence that Noonan syndrome (NS) and the cardio-facio-cutaneous syndrome (CFC) are variable manifestations of the same entity?M E Lorenzetti, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1995
Anal atresia and abdominal wall defect as unusual symptoms in EEC syndromeL De Smet, J P FrynsEuropean Journal of Obstetrics, Gynecology, and Reproductive Biology|February 16, 1999
Structural chromosome rearrangements in couples with recurrent fetal wastageJ P Fryns, G Van BuggenhoutAmerican Journal of Medical Genetics|April 1, 1992
Factors which contribute to cytogenetic frequency of expression in families of fragile X femalesG S Fisch, J P FrynsEuropean 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 FrynsActa Chirurgica Belgica|March 1, 1986
Carcinoid tumour of the thymus: a case reportG Deneffe, P MoermanPageof 89