A disease causing deletion of 29 base pairs in intron 15 in...

Clinical Genetics 2007 Vol. 72; Iss. 5

A disease causing deletion of 29 base pairs in intron 15 in the MKS1 gene is highly associated with the campomelic variant of the Meckel–Gruber syndrome

B Auber, P Burfeind, S Herold, K Schoner, G Simson, R Rauskolb, H Rehder
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Volume:
72
Year:
2007
Language:
english
Pages:
6
DOI:
10.1111/j.1399-0004.2007.00880.x
File:
PDF, 241 KB
english, 2007
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