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searching for Facioscapulohumeral muscular dystrophy 6 found (58 total)

alternate case: facioscapulohumeral muscular dystrophy

Cisca Wijmenga (619 words) [view diff] exact match in snippet view article find links to article

PhD at Leiden University in 1993 with a thesis titled: "Facioscapulohumeral muscular dystrophy: from genetic mapping towards gene cloning". In 1999 she
CRYM (1,041 words) [view diff] exact match in snippet view article find links to article
et al. (2007). "Abnormal expression of mu-crystallin in facioscapulohumeral muscular dystrophy". Exp. Neurol. 205 (2): 583–6. doi:10.1016/j.expneurol.2007
PDLIM3 (1,420 words) [view diff] exact match in snippet view article find links to article
specific actinin-associated LIM protein (ALP) gene from 4q35 facioscapulohumeral muscular dystrophy (FSHD) candidate genes". Neuromuscular Disorders. 9 (1):
ADP/ATP translocase 1 (1,138 words) [view diff] exact match in snippet view article find links to article
translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus". Human Genetics. 92 (2): 198–203. doi:10.1007/BF00219692
List of diseases (M) (2,469 words) [view diff] case mismatch in snippet view article
dystrophy congenital, merosin negative Muscular dystrophy, facioscapulohumeral Muscular dystrophy Hutterite type Muscular dystrophy limb girdle type 2A, Erb
Human genome (10,152 words) [view diff] exact match in snippet view article find links to article
CCDC28B and BBS1), Bardet-Biedl syndrome 10 (gene BBS10), and facioscapulohumeral muscular dystrophy type 2 (genes D4Z4 and SMCHD1). Genome sequencing is now