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Annales De Genetique|January 1, 1981
A malformed newborn with 9p and 4q trisomyJ P Fryns, M Azou, H Devliegher, et al.Human Genetics|January 1, 1981
Centromeric instability of chromosomes 1, 9, and 16 associated with combined immunodeficiencyJ P Fryns, M Azou, J Jaeken, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18pJ P Fryns, A Kleczkowska, K Devriendt, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Costello syndrome: a postnatal growth retardation syndrome with distinct phenotypeJ P Fryns, A Vogels, J Haegeman, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 1, 1984
Antenatal ultrasound diagnosis of fetal malformations: possibilities, limitations and dilemmasK Vandenberghe, F De Wolf, J P Fryns, et al.American Journal of Diseases of Children (1960)|September 1, 1984
Bloom's syndrome. Possible pitfalls in clinical diagnosisM Vanderschueren-Lodeweyckx, J P Fryns, H Van den Berghe, et al.Human Genetics|January 1, 1980
Perinatal mortality and XY/XX mosaicism. Report of two patientsJ P Fryns, M Haspeslagh, E Vandenbussche, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1991
X-linked mental retardation with Marfanoid habitus: a changing phenotype with age?J P Fryns, H Van Den BergheHuman Genetics|June 19, 1979
Congenital scalp defects associated with postaxial polydactylyJ P Fryns, H Van den BergheEuropean 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 BerghePageof 134