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Annales De Genetique|February 13, 2001
Cryptic translocation t(5;18) in familial mental retardationA Vogels, K Devriendt, J R Vermeesch, 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 FrynsArchives of Disease in Childhood. Fetal and Neonatal Edition|January 9, 2004
Pharmacokinetics of single dose intravenous propacetamol in neonates: effect of gestational ageK Allegaert, C D Van der Marel, A Debeer, et al.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 FrynsAmerican Journal of Medical Genetics|January 1, 1986
The female and the fragile X. A study of 144 obligate female carriersJ P FrynsActa Paediatrica (Oslo, Norway : 1992)|December 31, 2003
The respiratory pump: past and present understandingH DevliegerPageof 105