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Human Genetics|December 1, 1988
The pathology of trisomy 13 syndrome. A study of 12 casesP Moerman, J P Fryns, K van der Steen, et al.American Journal of Medical Genetics|May 1, 1988
Suggestively increased rate of infant death in children of fra(X) positive mothersJ P Fryns, P Moerman, F Gilis, et al.Clinical Genetics|July 1, 1987
Trisomy of the short arm of chromosome 5: autopsy data in a malformed newborn with inv dup (5) (p13.1----p15.3)A Kleczkowska, J P Fryns, P Moerman, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Non-immune hydrops fetalis caused by beta-glucuronidase deficiency (mucopolysaccharidosis VII). Study of a family with 3 affected siblingsJ Van Dorpe, P Moerman, A Pecceu, et al.American Journal of Medical Genetics|December 26, 2001
Bilateral tibial agenesis with ectrodactyly (OMIM 119100): further evidence for autosomal recessive inheritanceI Witters, K Devriendt, P Moerman, et al.American Journal of Medical Genetics|March 1, 1990
Pathogenesis of the lethal multiple pterygium syndromeP Moerman, J P Fryns, A Cornelis, et al.Annales De Genetique|January 1, 1987
Double autosomal trisomy (1q21.2----qter and 14pter----q13) in a female fetus with nuchal oedemaJ P Fryns, A Kleczkowska, P Moerman, et al.Annales De Genetique|January 1, 1987
The Roberts tetraphocomelia syndrome: identical limb defects in two siblingsJ P Fryns, A Kleczkowska, P Moerman, et al.American Journal of Medical Genetics|January 25, 2002
MCA syndrome with renal-hepatic-pancreatic dysplasia, posterior fossa cyst, symmetrical limb deficiencies, cleft palate, cardiac and Müllerian duct anomaliesI Witters, K Devriendt, D Spinnewijn, et al.Clinical Genetics|September 1, 1987
Type III congenital cystic adenomatoid malformation of the lung: another cause of elevated alpha fetoprotein?P Petit, M Bossens, D Thomas, et al.Pageof 89