domingo, 6 de enero de 2019

Genetic testing - OMIM - NCBI

Genetic testing - OMIM - NCBI

DNA testing concept with DNA strand and magnifier.

From NIH OMIM

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.



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XERODERMA PIGMENTOSUM, TYPE G/COCKAYNE SYNDROME, INCLUDED; XPG/CS, INCLUDED
Cytogenetic locations: 13q33.1
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Cytogenetic locations: 1pter-p36.13, 22q12.3, 1pter-p36.13, 22q11.21, 1pter-p36.13, 22q11.21, 1pter-p36.13, 1q32.1, 1pter-p36.13, 18p, 1pter-p36.13, 1p36.2, 1pter-p36.13, 14q32.33, 1pter-p36.13, 13q33.2, 1pter-p36.13, 13q32, 1pter-p36.13, 13q14.1pter-p36.13, 22q12.3, 1pter-p36.13, 22q11.21, 1pter-p36.13, 22q11.21, 1pter-p36.13, 1q32.1, 1pter-p36.13, 18p, 1pter-p36.13, 1p36.2, 1pter-p36.13, 14q32.33, 1pter-p36.13, 13q33.2, 1pter-p36.13, 13q32, 1pter-p36.13, 13q1

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