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American Journal of Medical Genetics|April 1, 1992
Aarskog syndrome: the changing phenotype with ageJ P FrynsJournal De Genetique Humaine|January 1, 1988
[Balanced chromosome abnormalities with abnormal phenotype]J P FrynsClinical Genetics|April 1, 1997
Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father. Clinical variability of 22q11 deletionK Devriendt, R Van Hoestenberghe, C Van Hole, et al.American Journal of Medical Genetics|January 1, 1986
The female and the fragile X. A study of 144 obligate female carriersJ P FrynsPrenatal Diagnosis|March 4, 1998
Polyhydramnios as a prenatal symptom of the digeorge/velo-cardio-facial syndromeK Devriendt, D Van Schoubroeck, B Eyskens, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Corpus callosum agenesis in Coffin-Lowry syndromeD Soekarman, J P FrynsGenetic Counseling (Geneva, Switzerland)|February 1, 2003
The Prader-Willi syndrome and the Angelman syndromeA Vogels, J P FrynsAmerican Journal of Medical Genetics|October 1, 1987
X-linked mental retardation with marfanoid habitusJ P Fryns, M ButtiensGenetic Counseling (Geneva, Switzerland)|January 1, 1994
Normal/trisomy 13 mosaicism in a 38-year-old maleP Petit, J P FrynsPageof 89