Showing results (271-280 of 883) with videos related to
Sort By:
Pageof 89
Human Genetics|September 1, 1988
X-chromosome polysomy in the male. The Leuven experience 1966-1987A Kleczkowska, J P Fryns, H Van den BergheClinical Genetics|January 1, 1988
De novo 3q/7q translocation and associated interstitial 7q35 deletionJ P Fryns, A Kleczkowska, H van den BergheAnnales De Genetique|January 1, 1987
Moderate mental retardation and mild dysmorphic syndrome in proximal 7q interstitial deletionJ P Fryns, A Kleczkowska, H Van den BergheJournal De Genetique Humaine|January 1, 1988
[Chromosome X-linked mental retardation and marfanoid syndrome]J P Fryns, M Buttiens, H van den BergheHuman Genetics|April 5, 1979
Partial trisomy of the short arm of chromosome 3 (3p25 to 3pter). A distinct clinical entityC Parloir, J P Fryns, H Van den BergheAnnales De Genetique|January 1, 1979
Partial trisomy 22q with elevated arylsulfatase-A activityJ P Fryns, J Jaeken, H van den BergheEuropean Journal of Pediatrics|June 1, 1988
Multiple pterygium syndrome type Escobar in two brothers. Follow-up data from childhood to adulthoodJ P Fryns, P Volcke, H van den BerghePediatric Pathology & Laboratory Medicine : Journal of the Society for Pediatric Pathology, Affiliated with the International Paediatric Pathology Association|July 1, 1997
Lymphangiomatosis of the body wall: a report of two cases associated with chylothorax and fatal outcomeP Moerman, C Van Geet, H DevliegerHuman Genetics|November 16, 1978
Unusual in vivo rearrangements of the Y chromosome with mitotic instability in vitroJ P Fryns, J J Cassiman, H Van den BergheClinical Genetics|April 19, 2011
Holoprosencephaly and ZIC2 microdeletions: novel clinical and epidemiological specificities delineatedE Chabchoub, D Willekens, J R Vermeesch, et al.Pageof 89