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Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Goldston syndrome reconsideredP Moerman, P Pauwels, K Vandenberghe, et al.Human Genetics|January 1, 1982
The Meckel Syndrome. Pathological and cytogenetic observations in eight casesP Moerman, E Verbeken, J P Fryns, et al.Journal of Medical Genetics|May 1, 1997
Chromosome 22q11 deletion presenting as the Potter sequenceK Devriendt, P Moerman, D Van Schoubroeck, et al.Prenatal Diagnosis|May 23, 2000
Diaphragmatic hernia as the first echographic sign in Apert syndromeI Witters, K Devriendt, P Moerman, et al.American Journal of Medical Genetics|August 28, 1995
Apparently new "anophthalmia-plus" syndrome in sibsJ P Fryns, E Legius, P Moerman, et al.Pediatric Pathology|May 1, 1994
Hereditary renal adysplasia: new observations and hypothesesP Moerman, J P Fryns, S H Sastrowijoto, et al.Annales De Genetique|January 1, 1988
The fetal phenotype in 15q2 duplicationJ P Fryns, A Kleczkowska, P Moerman, et al.Prenatal Diagnosis|August 1, 1994
Prenatal ultrasound diagnosis of rhizomelic chondrodysplasia punctata in a primigravidaS H Sastrowijoto, K Vandenberghe, P Moerman, et al.Annales De Genetique|January 1, 1990
Holoprosencephaly in a fetus with a 46,XX,der(7), t(7;8)(q36.1;p12) mat karyotypeA Kleczkowska, J P Fryns, P Moerman, et al.Clinical Genetics|October 1, 1983
Aberrant twinning (diprosopus) associated with anencephalyP Moerman, J P Fryns, P Goddeeris, et al.Pageof 89