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Annales 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 BergheTijdschrift Voor Psychiatrie|October 9, 2010
[Sleep disturbances in Smith-Magenis syndrome: treatment with melatonin and beta-adrenergic antagonists]A Van Thillo, K Devriendt, D WillekensPhysical Review. E|January 20, 2018
Pseudoinverse of the Laplacian and best spreader node in a networkP Van Mieghem, K Devriendt, H CetinayJournal of Medical Genetics|September 18, 2007
Genotype-phenotype correlation in 21 patients with Wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH)N M C Maas, G Van Buggenhout, F Hannes, et al.Disability and Rehabilitation|November 27, 2002
Disability in an urban black community in ZimbabweJ Jelsma, J Mielke, G Powell, et al.Journal De Genetique Humaine|March 1, 1982
Spectrum of clinical and autopsy findings in trisomy 18 syndromeP Moerman, J P Fryns, P Goddeeris, et al.Pageof 90