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Clinical 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 Human Genetics|March 1, 1997
Skewed X-chromosome inactivation in female carriers of dyskeratosis congenitaK Devriendt, G Matthijs, E Legius, et al.Cytogenetic and Genome Research|November 25, 2006
Molecular karyotyping of patients with MCA/MR: the blurred boundary between normal and pathogenic variationT J L de Ravel, I Balikova, B Thienpont, et al.Genetic Counseling (Geneva, Switzerland)|January 5, 2001
MCA/MR syndrome with severe pre- and postnatal growth retardation, deep mental retardation, distinct facial appearance with nasal hypoplasia, cleft palate and retino-choroidal coloboma in two unrelated female patientsJ P FrynsAmerican 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 FrynsAmerican Journal of Medical Genetics|January 1, 1986
The female and the fragile X. A study of 144 obligate female carriersJ P FrynsJournal of Medical Genetics|May 1, 1997
Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndromeK Devriendt, P Petit, G Matthijs, et al.Prenatal Diagnosis|March 4, 1998
Polyhydramnios as a prenatal symptom of the digeorge/velo-cardio-facial syndromeK Devriendt, D Van Schoubroeck, B Eyskens, et al.Pageof 90