Human NDUFB9 Gene: Genomic Organization and a Possible Candidate Gene Associated with Deafness Disorder Mapped to Chromosome 8q13.
- Published in:
- Human Heredity, 1999, v. 49, n. 2, p. 75, doi. 10.1159/000022848
- By:
- Publication type:
- Article
Works matching IS 00015652 AND DT 1999 AND VI 49 AND IP 2
Results: 12
1
2
Analysis of the Complete Coding Region of the CFTR Gene in Ten Algerian Cystic Fibrosis Families.
- Published in:
- Human Heredity, 1999, v. 49, n. 2, p. 81, doi. 10.1159/000022849
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- Publication type:
- Article
3
Molecular Genetic Study of Autosomal Dominant Retinitis pigmentosa in Lithuanian Patients.
- Published in:
- Human Heredity, 1999, v. 49, n. 2, p. 71, doi. 10.1159/000022847
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- Publication type:
- Article
4
Contribution of Interleukin 1β and KM Loci to Alopecia areata.
- Published in:
- Human Heredity, 1999, v. 49, n. 2, p. 85, doi. 10.1159/000022850
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- Publication type:
- Article
5
Hereditary Desmoid Disease in a Family with a Germline Alu I Repeat Mutation of the APC Gene.
- Published in:
- Human Heredity, 1999, v. 49, n. 2, p. 97, doi. 10.1159/000022852
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- Publication type:
- Article
6
Linkage Disequilibrium and Haplotype Analysis in German Friedreich Ataxia Families.
- Published in:
- Human Heredity, 1999, v. 49, n. 2, p. 90, doi. 10.1159/000022851
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- Publication type:
- Article
7
A Principal-Components Approach Based on Heritability for Combining Phenotype Information.
- Published in:
- Human Heredity, 1999, v. 49, n. 2, p. 106, doi. 10.1159/000022854
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- Publication type:
- Article
8
No Correlation between A(-1438)G Polymorphism in 5-HT2A Receptor Gene Promoter and the Density of Frontal Cortical 5-HT2A Receptors in Schizophrenia.
- Published in:
- Human Heredity, 1999, v. 49, n. 2, p. 103, doi. 10.1159/000022853
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- Publication type:
- Article
9
Linkage Information Content of Polymorphic Genetic Markers.
- Published in:
- Human Heredity, 1999, v. 49, n. 2, p. 112, doi. 10.1159/000022855
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- Publication type:
- Article
10
A Novel Splice Site Mutation in a Brazilian Patient with Hereditary Antithrombin Deficiency Type I.
- Published in:
- Human Heredity, 1999, v. 49, n. 2, p. 119, doi. 10.1159/000022856
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- Publication type:
- Article
11
A Novel Nonsense Mutation 6, E - X in the Protein S Gene Causes Type I Deficiency.
- Published in:
- Human Heredity, 1999, v. 49, n. 2, p. 121, doi. 10.1159/000022857
- By:
- Publication type:
- Article
12
True Pedigree Errors More Frequent Than Apparent Errors for Single Nucleotide Polymorphisms.
- Published in:
- Human Heredity, 1999, v. 49, n. 2, p. 65, doi. 10.1159/000022846
- By:
- Publication type:
- Article