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Genetic Counseling (Geneva, Switzerland)|July 28, 1999
Moderate mental retardation without dysmorphic symptoms in intrachromosomal 11p12 duplicationE Goossens, R Cayenberghs, J P FrynsAnnales De Genetique|August 6, 1999
A 3p deletion syndrome in a child with both del(3)(p25-->pter) and dup(17)(q23-->qter)T Lukusa, K Devriendt, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 13, 2000
On the association profound nerve deafness, semilobar holoprosencephaly, and minor midline developmental anomaliesG Vantrappen, L Feenstra, J P FrynsGenetic Counseling (Geneva, Switzerland)|October 24, 2000
Conductive hearing loss and multiple pre- and supra-auricular skin defects: a variant example of the Branchio-Oculo-Facial syndromeG Vantrappen, L Feenstra, J P FrynsGenetic Counseling (Geneva, Switzerland)|August 5, 2010
Preconception careI Witters, A Bogaerts, J P FrynsHuman Genetics|January 1, 1980
Sex-linked recessive inheritance in Charcot-Marie-tooth disease with partial clinical manifestations in female carriersJ P Fryns, H Van den BergheGenetic Counseling (Geneva, Switzerland)|May 3, 2001
Partial distal trisomy 3p. A partial autosomal trisomy without major dysmorphic featuresE Smeets, L Vandenbossche, J P FrynsAnnales De Genetique|January 1, 1984
De novo complex chromosomal rearrangement (CCR) in a severely mentally retarded boyJ P Fryns, A Kleczkowska, H KenisEuropean Journal of Pediatrics|June 28, 1979
Corneal clouding, subvalvular aortic stenosis, and midfacial hypoplasia associated with mental deficiency and growth retardation--a new syndrome?J P Fryns, H Van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1997
Pierre-Robin sequence and severe mental retardation with chaotic behaviour associated with a small interstitial deletion in the long arm of chromosome 2 (del(2)(q331q333))A Vogels, J Haegeman, J P FrynsPageof 89