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Volume 6; Issue 1
Main
Human Molecular Genetics
Volume 6; Issue 1
Human Molecular Genetics
Volume 6; Issue 1
1
Lack of founding Amerindian mitochondrial DNA lineages in extinct aborigines from Tierra del Fuego-Patagonia
Lalueza, C
Journal:
Human Molecular Genetics
Year:
1997
Language:
english
File:
PDF, 109 KB
Your tags:
english, 1997
2
A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21
Chaib, H
Journal:
Human Molecular Genetics
Year:
1997
Language:
english
File:
PDF, 125 KB
Your tags:
english, 1997
3
The IL-9 receptor gene, located in the Xq/Yq pseudoautosomal region, has an autosomal origin, escapes X inactivation and is expressed from the Y
Vermeesch, J.
Journal:
Human Molecular Genetics
Year:
1997
Language:
english
File:
PDF, 209 KB
Your tags:
english, 1997
4
Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysis
Sheffield, V.
Journal:
Human Molecular Genetics
Year:
1997
Language:
english
File:
PDF, 89 KB
Your tags:
english, 1997
5
Emergence and scattering of multiple neurofibromatosis (NF1)-related sequences during hominoid evolution suggest a process of pericentromeric interchromosomal transposition
Regnier, V
Journal:
Human Molecular Genetics
Year:
1997
Language:
english
File:
PDF, 187 KB
Your tags:
english, 1997
6
The BRC repeats are conserved in mammalian BRCA2 proteins
Bignell, G
Journal:
Human Molecular Genetics
Year:
1997
Language:
english
File:
PDF, 313 KB
Your tags:
english, 1997
7
Genotype-phenotype correlation for nucleotide substitutions in the IgII- IgIII linker of FGFR2
Oldridge, M
Journal:
Human Molecular Genetics
Year:
1997
Language:
english
File:
PDF, 241 KB
Your tags:
english, 1997
8
Somatic mutation processes at a human minisatellite
Jeffreys, A.
Journal:
Human Molecular Genetics
Year:
1997
Language:
english
File:
PDF, 238 KB
Your tags:
english, 1997
9
Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: lack of genotype/phenotype correlations
Meyer, J
Journal:
Human Molecular Genetics
Year:
1997
Language:
english
File:
PDF, 106 KB
Your tags:
english, 1997
10
Trinucleotide repeats in the human genome: size distributions for all possible triplets and detection of expanded disease alleles in a group of Huntington disease individuals by the repeat expansion detection method
Hofferbert, S
Journal:
Human Molecular Genetics
Year:
1997
Language:
english
File:
PDF, 136 KB
Your tags:
english, 1997
11
Cancer risk associated with germline DNA mismatch repair gene mutations
Dunlop, M.
Journal:
Human Molecular Genetics
Year:
1997
Language:
english
File:
PDF, 72 KB
Your tags:
english, 1997
12
Translation initiation factor eIF-4gamma is encoded by an amplified gene and induces an immune response in squamous cell lung carcinoma
Brass, N
Journal:
Human Molecular Genetics
Year:
1997
Language:
english
File:
PDF, 262 KB
Your tags:
english, 1997
13
Comparison of the human and mouse genes encoding the telomeric protein, TRF1: chromosomal localization, expression and conserved protein domains
Broccoli, D
Journal:
Human Molecular Genetics
Year:
1997
Language:
english
File:
PDF, 218 KB
Your tags:
english, 1997
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