From NIH OMIM
OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.
Cytogenetic locations: 16q24.1
- OMIM:
- 614893
2.
IMMUNODEFICIENCY 18, SEVERE COMBINED IMMUNODEFICIENCY VARIANT, INCLUDED
Cytogenetic locations: 11q23.3
- OMIM:
- 615615
3.
Cytogenetic locations: 16q24.1
- OMIM:
- 614894
4.
Cytogenetic locations: 16p12.1
- OMIM:
- 615207
5.
Cytogenetic locations: 7p22.2
- OMIM:
- 615206
6.
Cytogenetic locations: 1q24.2
- OMIM:
- 610163
7.
Cytogenetic locations: 1q42.3
- OMIM:
- 617765
8.
Cytogenetic locations: 14q32.2
- OMIM:
- 617237
9.
Cytogenetic locations: 2q37.1
- OMIM:
- 235550
10.
Cytogenetic locations: 11q23.3
- OMIM:
- 615617
11.
12.
Cytogenetic locations: Xq12
- OMIM:
- 300988
13.
Cytogenetic locations: 11q23.3
- OMIM:
- 615607
14.
Cytogenetic locations: 3q29
- OMIM:
- 616740
15.
Cytogenetic locations: 14q11.2
- OMIM:
- 615387
16.
Cytogenetic locations: 18q21.32
- OMIM:
- 615468
17.
Cytogenetic locations: 4q24
- OMIM:
- 616576
18.
Cytogenetic locations: 20p13
- OMIM:
- 615895
19.
Cytogenetic locations: 6q14.1
- OMIM:
- 615816
20.
Cytogenetic locations: 4q27
- OMIM:
- 615767
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