K Ricker|H G Mertens - JoVE Visualize

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Neurology|February 26, 2003

Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrumJ W Day, K Ricker, J F Jacobsen, et al.

Human Genetics|September 1, 1996

Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM intervalB Fontaine, S Nicole, H Topaloglu, et al.

Nature Genetics|June 30, 2001

Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle diseaseR C Betz, B G Schoser, D Kasper, et al.

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Showing results (91-100 of 93) with videos related to

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You have reached the last page of results.This site can display upto 93 results.

Neurology|February 26, 2003

Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrumJ W Day, K Ricker, J F Jacobsen, et al.

Human Genetics|September 1, 1996

Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM intervalB Fontaine, S Nicole, H Topaloglu, et al.

Nature Genetics|June 30, 2001

Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle diseaseR C Betz, B G Schoser, D Kasper, et al.

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