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Genetic Counseling (Geneva, Switzerland)|January 1, 1990
High incidence of mental retardation in Turner syndrome patients with ring chromosome X formationJ P Fryns, A Kleczkowska, H Van Den BergheJournal of Medical Genetics|August 1, 1989
Hypohidrotic ectodermal dysplasia, primary hypothyroidism, and agenesis of the corpus callosumJ P Fryns, K Chrzanowska, H Van den BergheAnnales De Genetique|January 1, 1995
Renal agenesis and trisomy 22: case report and reviewG J Van Buggenhout, J Verbruggen, J P FrynsEuropean Journal of Human Genetics : EJHG|October 22, 1998
Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large familyE Legius, E Schollen, G Matthijs, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Partial trisomy 4q due to a maternal translocation: t(4;18)(q27;q21.31)G Van Buggenhout, P H Moerman, J P FrynsJournal De Genetique Humaine|March 1, 1980
Diaphragmatic defects, craniofacial dysmorphism, cleft palate and distal limb deformities. - a new lethal syndromeP Goddeeris, J P Fryns, H van den BergheGynecologic Oncology|December 1, 1995
Meigs' syndrome with elevated serum CA 125 levels: two case reports and review of the literatureD Timmerman, P Moerman, I VergoteAnnales De Genetique|January 1, 1986
47,XXY karyotype in a patient with Beckwith-Wiedemann syndromeJ P Fryns, A Kleczkowska, H Van den BergheAnnales De Genetique|January 1, 1990
Interstitial deletion of the short arm of chromosome 12. Report of a new patient and review of the literatureJ P Fryns, A Kleczkowska, H Van den BergheClinical Genetics|December 1, 1991
Cohen syndrome: fertility in a female patientJ P Fryns, F Lemmens, H van den BerghePageof 89