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Human Molecular Genetics
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April 30, 2002
Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy
José M Morante-Redolat, Ana Gorostidi-Pagola, Salomé Piquer-Sirerol, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 12, 2007
Germline NF1 mutational spectra and loss-of-heterozygosity analyses in patients with pheochromocytoma and neurofibromatosis type 1
Birke Bausch, Wiktor Borozdin, Victor F Mautner, et al.
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Search research articles
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Showing results (71-80 of 72) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 72 results.
Human Molecular Genetics
|
April 30, 2002
Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy
José M Morante-Redolat, Ana Gorostidi-Pagola, Salomé Piquer-Sirerol, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 12, 2007
Germline NF1 mutational spectra and loss-of-heterozygosity analyses in patients with pheochromocytoma and neurofibromatosis type 1
Birke Bausch, Wiktor Borozdin, Victor F Mautner, et al.
Page
of 8