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Genetic Counseling (Geneva, Switzerland)|August 2, 2002
Oculo-dento-digital dysplasia (OMIM *164200). Full manifestation of the syndrome in a 9.5 year-old girl and type III syndactyly in the fatherD M Ioan, D Dagomiz, J P FrynsGenetic Counseling (Geneva, Switzerland)|July 14, 2000
Three young children with Smith-Magenis syndrome: their distinct, recognisable behavioural phenotype as the most important clinical symptomsD Willekens, P De Cock, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 5, 2001
Cytomegalovirus reactivation in pregnancy and subsequent isolated bilateral hearing loss in the infantI Witters, M Van Ranst, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1992
Radial ray deficiency and ulnar ray deficiency in two sibsL De Smet, G Fabry, J P FrynsGenetic Counseling (Geneva, Switzerland)|November 6, 2001
Further evidence for germinal mosaicism in cleft hand/cleft foot syndrome. Two affected halfsisters and normal fatherL De Smet, K Devriendt, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1996
Costello syndrome: report of an 8-month-old marasmic boyM Popa, D M Ioan, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1995
Craniofrontonasal dysplasia: more severe expression in the mother than in her sonK Devriendt, C Van Mol, J P FrynsGenetic Counseling (Geneva, Switzerland)|February 12, 2002
Intrafamilial clinical variability in type C brachydactylyP Debeer, L De Smet, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1992
A syndrome of mental retardation, short stature, craniofacial anomalies with palpebral ptosis and pulmonary stenosis in three siblings with normal parents. An example of autosomal recessive inheritance of the Noonan phenotype?C Maximilian, D M Ioan, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1992
Madelung deformity as a pathognomonic feature of the onycho-osteodysplasia syndromeD M Ioan, C Maximilian, J P FrynsPageof 89