Volume 6; Issue 1

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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

Journal:

Human Molecular Genetics

Year:

1997

Language:

english

File:

PDF, 109 KB

english, 1997

2

A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21

Journal:

Human Molecular Genetics

Year:

1997

Language:

english

File:

PDF, 125 KB

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

Journal:

Human Molecular Genetics

Year:

1997

Language:

english

File:

PDF, 209 KB

english, 1997

4

Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysis

Journal:

Human Molecular Genetics

Year:

1997

Language:

english

File:

PDF, 89 KB

english, 1997

5

Emergence and scattering of multiple neurofibromatosis (NF1)-related sequences during hominoid evolution suggest a process of pericentromeric interchromosomal transposition

Journal:

Human Molecular Genetics

Year:

1997

Language:

english

File:

PDF, 187 KB

english, 1997

6

The BRC repeats are conserved in mammalian BRCA2 proteins

Journal:

Human Molecular Genetics

Year:

1997

Language:

english

File:

PDF, 313 KB

english, 1997

7

Genotype-phenotype correlation for nucleotide substitutions in the IgII- IgIII linker of FGFR2

Journal:

Human Molecular Genetics

Year:

1997

Language:

english

File:

PDF, 241 KB

english, 1997

8

Somatic mutation processes at a human minisatellite

Journal:

Human Molecular Genetics

Year:

1997

Language:

english

File:

PDF, 238 KB

english, 1997

9

Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: lack of genotype/phenotype correlations

Journal:

Human Molecular Genetics

Year:

1997

Language:

english

File:

PDF, 106 KB

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

Journal:

Human Molecular Genetics

Year:

1997

Language:

english

File:

PDF, 136 KB

english, 1997

11

Cancer risk associated with germline DNA mismatch repair gene mutations

Journal:

Human Molecular Genetics

Year:

1997

Language:

english

File:

PDF, 72 KB

english, 1997

12

Translation initiation factor eIF-4gamma is encoded by an amplified gene and induces an immune response in squamous cell lung carcinoma

Journal:

Human Molecular Genetics

Year:

1997

Language:

english

File:

PDF, 262 KB

english, 1997

13

Comparison of the human and mouse genes encoding the telomeric protein, TRF1: chromosomal localization, expression and conserved protein domains

Journal:

Human Molecular Genetics

Year:

1997

Language:

english

File:

PDF, 218 KB

english, 1997