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American Journal of Medical Genetics|August 9, 1996
Fragile X mutation and FG syndrome-like phenotypeC Piussan, M Mathieu, P Berquin, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1996
The Floating-Harbor syndrome: report of another patient and differential diagnosis with Shprintzen syndromeE Smeets, J P Fryns, H Van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1995
Severe axial mesodermal dysplasia spectrum in an infant of a diabetic motherM Depraetere, R Dehauwere, P Mariën, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|September 1, 1989
X-to-X translocation associated with gonadal dysgenesis and discrete Turner syndrome stigmata; a case reportA Kleczkowska, J P Fryns, H Van den BergheAnnales De Genetique|January 1, 1992
Trisomy of the short arm of chromosome 4: the changing phenotype with ageA Kleczkowska, J P Fryns, H van den BergheClinical Genetics|December 1, 1992
Posterior scalp defects in Opitz syndrome. Another symptom related to a defect in midline developmentJ P Fryns, J Delooz, H van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1994
Catel-Manzke palatodigital syndrome in a second trimester female foetus with nuchal oedema, costovertebral anomalies and radial ray defectP Petit, P Moerman, E Legius, et al.European Journal of Pediatrics|October 1, 1983
Familial infantile cortical hyperostosisL Emmery, J Timmermans, J Christens, et al.Annales De Genetique|August 26, 1998
Partial trisomy 1q (1q32-->1qter) in adulthood: further delineation of the phenotypeG Van Buggenhout, L De Coen, J P FrynsClinical Genetics|March 1, 1997
Prenatal growth retardation, microphthalmos/iris coloboma, cloudy cornea, urogenital anomalies and microcephaly. A possible new sublethal syndromeJ P Fryns, H Verresen, H Van den BerghePageof 90