skip to main content
Language:
Search Limited to: Search Limited to: Resource type Show Results with: Show Results with: Search type Index

Results 1 - 20 of 104  for All Library Resources

Results 1 2 3 4 5 next page
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Population Demographic History Can Cause the Appearance of Recombination Hotspots
Material Type:
Article
Add to My Research

Population Demographic History Can Cause the Appearance of Recombination Hotspots

American journal of human genetics, 2012-05, Vol.90 (5), p.774-783 [Peer Reviewed Journal]

2012 The American Society of Human Genetics ;2015 INIST-CNRS ;Copyright © 2012 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press May 4, 2012 ;2012 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2012 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2012.03.011 ;PMID: 22560089 ;CODEN: AJHGAG

Full text available

2
Relationship between Deleterious Variation, Genomic Autozygosity, and Disease Risk: Insights from The 1000 Genomes Project
Material Type:
Article
Add to My Research

Relationship between Deleterious Variation, Genomic Autozygosity, and Disease Risk: Insights from The 1000 Genomes Project

American journal of human genetics, 2018-04, Vol.102 (4), p.658-675 [Peer Reviewed Journal]

2018 American Society of Human Genetics ;Copyright © 2018 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;2018 American Society of Human Genetics. 2018 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2018.02.013 ;PMID: 29551419

Full text available

3
mtDNA variation of aboriginal Siberians reveals distinct genetic affinities with Native Americans
Material Type:
Article
Add to My Research

mtDNA variation of aboriginal Siberians reveals distinct genetic affinities with Native Americans

American journal of human genetics, 1993-09, Vol.53 (3), p.591-608 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 7688933 ;CODEN: AJHGAG

Full text available

4
Slow acetylator mutations in the human polymorphic N-acetyltransferase gene in 786 Asians, blacks, Hispanics, and whites : application to metabolic epidemiology
Material Type:
Article
Add to My Research

Slow acetylator mutations in the human polymorphic N-acetyltransferase gene in 786 Asians, blacks, Hispanics, and whites : application to metabolic epidemiology

American journal of human genetics, 1993-04, Vol.52 (4), p.827-834 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 8460648 ;CODEN: AJHGAG

Full text available

5
The Gender-specific apolipoprotein E genotype influence on the distribution of plasma lipids and apolipoproteins in the population of Rochester, Minnesota. II: Regression relationships with concomitants
Material Type:
Article
Add to My Research

The Gender-specific apolipoprotein E genotype influence on the distribution of plasma lipids and apolipoproteins in the population of Rochester, Minnesota. II: Regression relationships with concomitants

American journal of human genetics, 1992-12, Vol.51 (6), p.1311-1324 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 1463013 ;CODEN: AJHGAG

Full text available

6
Polymorphic haplotypes and recombination rates at the LDL receptor gene locus in subjects with and without familial hypercholesterolemia who are from different populations
Material Type:
Article
Add to My Research

Polymorphic haplotypes and recombination rates at the LDL receptor gene locus in subjects with and without familial hypercholesterolemia who are from different populations

American journal of human genetics, 1993-04, Vol.52 (4), p.808-826 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 8096361 ;CODEN: AJHGAG

Full text available

7
Asian affinities and continental radiation of the four founding native American mtDNAs
Material Type:
Article
Add to My Research

Asian affinities and continental radiation of the four founding native American mtDNAs

American journal of human genetics, 1993-09, Vol.53 (3), p.563-590 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 7688932 ;CODEN: AJHGAG

Full text available

8
mtDNA and Y-chromosome polymorphisms in four native American populations from Southern Mexico
Material Type:
Article
Add to My Research

mtDNA and Y-chromosome polymorphisms in four native American populations from Southern Mexico

American journal of human genetics, 1994-02, Vol.54 (2), p.303-318 [Peer Reviewed Journal]

1994 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 8304347 ;CODEN: AJHGAG

Full text available

9
Anticipation in bipolar affective disorder
Material Type:
Article
Add to My Research

Anticipation in bipolar affective disorder

American journal of human genetics, 1993-08, Vol.53 (2), p.385-390 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 8328456 ;CODEN: AJHGAG

Full text available

10
Analysis of HLA class II haplotypes in the Cayapa Indians of Ecuador : a novel DRBI allele reveals evidence for convergent evolution and balancing selection at position 86
Material Type:
Article
Add to My Research

Analysis of HLA class II haplotypes in the Cayapa Indians of Ecuador : a novel DRBI allele reveals evidence for convergent evolution and balancing selection at position 86

American journal of human genetics, 1994-07, Vol.55 (1), p.160-167 [Peer Reviewed Journal]

1994 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;CODEN: AJHGAG

Full text available

11
Linkage and mutational analysis of familial alzheimer disease kindreds for the APP gene region
Material Type:
Article
Add to My Research

Linkage and mutational analysis of familial alzheimer disease kindreds for the APP gene region

American journal of human genetics, 1992-11, Vol.51 (5), p.998-1014 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 1415269 ;CODEN: AJHGAG

Full text available

12
Most of rare missense alleles in humans are deleterious:implications for evolution of complex disease and associationstudies
Material Type:
Article
Add to My Research

Most of rare missense alleles in humans are deleterious:implications for evolution of complex disease and associationstudies

American journal of human genetics, 2006-10, Vol.80 [Peer Reviewed Journal]

ISSN: 0002-9297 ;EISSN: 1537-6605

Full text available

13
The Y alu polymorphism in southern African populations and its relationship to other Y-specific polymorphisms
Material Type:
Article
Add to My Research

The Y alu polymorphism in southern African populations and its relationship to other Y-specific polymorphisms

American journal of human genetics, 1994-02, Vol.54 (2), p.319-330 [Peer Reviewed Journal]

1994 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 8304348 ;CODEN: AJHGAG

Full text available

14
Extended multipoint identity-by-descent analysis of human quantitative traits : efficiency, power, and modeling considerations
Material Type:
Article
Add to My Research

Extended multipoint identity-by-descent analysis of human quantitative traits : efficiency, power, and modeling considerations

American journal of human genetics, 1993-12, Vol.53 (6), p.1306-1319 [Peer Reviewed Journal]

1994 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 8250047 ;CODEN: AJHGAG

Full text available

15
Network Analyses of Y-Chromosomal Types in Europe, Northern Africa, and Western Asia Reveal Specific Patterns of Geographic Distribution
Material Type:
Article
Add to My Research

Network Analyses of Y-Chromosomal Types in Europe, Northern Africa, and Western Asia Reveal Specific Patterns of Geographic Distribution

American journal of human genetics, 1998-09, Vol.63 (3), p.847-860 [Peer Reviewed Journal]

1998 The American Society of Human Genetics ;1998 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/301999 ;PMID: 9718330 ;CODEN: AJHGAG

Full text available

16
The genetics of XX gonadal dysgenesis
Material Type:
Article
Add to My Research

The genetics of XX gonadal dysgenesis

American journal of human genetics, 1994-05, Vol.54 (5), p.844-851 [Peer Reviewed Journal]

1994 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 8178824 ;CODEN: AJHGAG

Full text available

17
Characteristics of polymorphism at a VNTR locus 3' to the apolipoprotein B gene in five human populations
Material Type:
Article
Add to My Research

Characteristics of polymorphism at a VNTR locus 3' to the apolipoprotein B gene in five human populations

American journal of human genetics, 1992-12, Vol.51 (6), p.1325-1333 [Peer Reviewed Journal]

ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 1463014

Full text available

18
Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe disease
Material Type:
Article
Add to My Research

Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe disease

American journal of human genetics, 1992-01, Vol.50 (1), p.222-228 [Peer Reviewed Journal]

ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 1370365

Full text available

19
Multiple origins for phenylketonuria in Europe
Material Type:
Article
Add to My Research

Multiple origins for phenylketonuria in Europe

American journal of human genetics, 1992-12, Vol.51 (6), p.1355-1365 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 1361100 ;CODEN: AJHGAG

Full text available

20
Further evidence for a locus for cutaneous malignant melanoma-dysplastic nevus (CMM/DN) on chromosome Ip, and evidence for genetic heterogeneity
Material Type:
Article
Add to My Research

Further evidence for a locus for cutaneous malignant melanoma-dysplastic nevus (CMM/DN) on chromosome Ip, and evidence for genetic heterogeneity

American journal of human genetics, 1993-03, Vol.52 (3), p.537-550 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;CODEN: AJHGAG

Full text available

Results 1 - 20 of 104  for All Library Resources

Results 1 2 3 4 5 next page

Personalize your results

  1. Edit

Refine Search Results

Expand My Results

  1.   

Refine My Results

Creation Date 

From To
  1. Before 1992  (3)
  2. 1992 To 1993  (74)
  3. 1994 To 1998  (24)
  4. 1999 To 2012  (3)
  5. After 2012  (1)
  6. More options open sub menu

Searching Remote Databases, Please Wait