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Annales De Genetique|May 26, 1998
Unusual de novo t(13;15)(q12.1;p13) translocation leading to complex mosaicism including jumping translocationP Petit, K Devriendt, J R Vermeesch, et al.
Annales De Genetique|January 1, 1987
Distinct dysmorphic syndrome in a child with inverted distal 5q duplicationJ P Fryns, A Kleczkowska, M Borghgraef, et al.
Genetic Counseling (Geneva, Switzerland)|April 7, 1999
Retrospective analysis of feeding and speech disorders in 50 patients with velo-cardio-facial syndromeN Rommel, G Vantrappen, A Swillen, et al.
Human Genetics|January 1, 1984
Cytogenetic survey in couples with recurrent fetal wastageJ P Fryns, A Kleczkowska, E Kubień, et al.
Genetic Counseling (Geneva, Switzerland)|October 20, 1998
Spasticity, mental retardation, macrocephaly and distinct craniofacial appearance: confirmation of a new subtype of complicated spastic paraplegia?U Moog, A M Schoonbrood-Lenssen, C T Schrander-Stumpel, et al.
American Journal of Human Genetics|November 9, 2000
Primary autosomal recessive microcephaly: MCPH5 maps to 1q25-q32C R Jamieson, J P Fryns, J Jacobs, et al.
Journal of Mental Deficiency Research|June 1, 1990
The 49,XXXXY syndrome: clinical and psychological findings in five patientsL M Curfs, G Schreppers-Tijdink, A Wiegers, et al.
Clinical Genetics|March 1, 1987
Tetraploidy with hydrops fetalis, cystic nuchal hygroma and 90, XX karyotypeJ P Fryns, K Vandenberghe, F Moerman, et al.
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