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American Journal of Human Genetics|October 30, 1998
X chromosome inactivation in carriers of Barth syndromeK H Orstavik, R E Orstavik, A K Naumova, et al.
Neuromuscular Disorders : NMD|June 3, 1998
Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery-Dreifuss muscular dystrophy patients and carriersP Sabatelli, S Squarzoni, S Petrini, et al.
Nucleic Acids Research|May 25, 1991
Molecular cloning and analysis of the fragile X region in manA Dietrich, P Kioschis, A P Monaco, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 23, 1996
A family of transmembrane proteins with homology to the MET-hepatocyte growth factor receptorE Maestrini, L Tamagnone, P Longati, et al.
Science (New York, N.Y.)|March 8, 1991
Isolation of sequences that span the fragile X and identification of a fragile X-related CpG islandD Heitz, F Rousseau, D Devys, et al.
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