Expression patterns common and unique to ulcerative colitis and celiac disease.
- Published in:
- Annals of Human Genetics, 2019, v. 83, n. 2, p. 86, doi. 10.1111/ahg.12293
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- Publication type:
- Article
Works matching IS 00034800 AND DT 2019 AND VI 83 AND IP 2
Results: 7
1
2
Genetic variations and population data on five supplementary STR markers in Lebanon.
- Published in:
- Annals of Human Genetics, 2019, v. 83, n. 2, p. 82, doi. 10.1111/ahg.12292
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- Publication type:
- Article
3
IL8 and IL17A polymorphisms associated with multibacillary leprosy and reaction type 1 in a mixed population from southern Brazil.
- Published in:
- Annals of Human Genetics, 2019, v. 83, n. 2, p. 110, doi. 10.1111/ahg.12291
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- Publication type:
- Article
4
Confirmation of BRD4 haploinsufficiency role in Cornelia de Lange–like phenotype and delineation of a 19p13.12p13.11 gene contiguous syndrome.
- Published in:
- Annals of Human Genetics, 2019, v. 83, n. 2, p. 100, doi. 10.1111/ahg.12289
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- Publication type:
- Article
5
DYNC1H1 gene methylation correlates with severity of spinal muscular atrophy.
- Published in:
- Annals of Human Genetics, 2019, v. 83, n. 2, p. 73, doi. 10.1111/ahg.12288
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- Publication type:
- Article
6
A novel heterozygous variant p.(Trp538Arg) of SYNM is identified by whole‐exome sequencing in a Chinese family with dilated cardiomyopathy.
- Published in:
- Annals of Human Genetics, 2019, v. 83, n. 2, p. 95, doi. 10.1111/ahg.12287
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- Publication type:
- Article
7
Issue Information.
- Published in:
- Annals of Human Genetics, 2019, v. 83, n. 2, p. 1, doi. 10.1111/ahg.12266
- Publication type:
- Article