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Genetic Counseling (Geneva, Switzerland)|February 26, 2009
Unilateral radio-ulnar synostosis and idic-Y chromosomeL De Smet, J P FrynsGenetic Counseling (Geneva, Switzerland)|July 28, 1999
The neurobiology of autismS T Potgieter, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1991
Oculocerebral syndrome with hypopigmentation (Cross syndrome): the mixed pattern of hair pigmentation as an important diagnostic signG De Jong, J P FrynsGenetic Counseling (Geneva, Switzerland)|November 6, 2002
Costello syndrome in two siblings and minor manifestations in their mother. Further evidence for autosomal dominant inheritance?D M Ioan, J P FrynsClinical Dysmorphology|October 1, 1994
On the association of Poland anomaly and primary microcephalyJ P Fryns, L de SmetAmerican 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 FrynsHuman Genetics|February 28, 2003
PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouseH Peeters, P Debeer, A Bairoch, et al.Pageof 90