From NIH OMIM
OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.
1.
Cytogenetic locations: 22q13.1
- OMIM:
- 607109
2.
Cytogenetic locations: 22q13.1
- OMIM:
- 610976
3.
Cytogenetic locations: 22q13.1
- OMIM:
- 607750
4.
Cytogenetic locations: 12p13.31
- OMIM:
- 600130
5.
Cytogenetic locations: 22q13.1
- OMIM:
- 607110
6.
Cytogenetic locations: 22q13.1
- OMIM:
- 607113
7.
Cytogenetic locations: 16q22.1
- OMIM:
- 601065
8.
Cytogenetic locations: 17q21.31
- OMIM:
- 613212
9.
Cytogenetic locations: 17q11.2
- OMIM:
- 613113
10.
Cytogenetic locations: 20q13.31
- OMIM:
- 606750
11.
Cytogenetic locations: 12p13.31
- OMIM:
- 605257
12.
POU5F1/EWS FUSION GENE, INCLUDED
Cytogenetic locations: 6p21.33
- OMIM:
- 164177
13.
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE, INCLUDED
Cytogenetic locations: 1pter-p36.13, 22q12.2, 1pter-p36.13, 21q22.11
- OMIM:
- 105400
14.
HEMOPHILIA B(M), INCLUDED
Cytogenetic locations: Xq27.1
- OMIM:
- 306900
15.
APO-DYSTROPHIN 1, INCLUDED
Cytogenetic locations: Xp21.2-p21.1
- OMIM:
- 300377
16.
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 1, INCLUDED; MC5DM1, INCLUDED
- OMIM:
- 516060
17.
PRKAR1A/RARA FUSION GENE, INCLUDED
Cytogenetic locations: 17q24.2
- OMIM:
- 188830
18.
Cytogenetic locations: 9p21.2
- OMIM:
- 617119
19.
Cytogenetic locations: 17q23.3
- OMIM:
- 601736
20.
Cytogenetic locations: 3q13.33
- OMIM:
- 602500
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