(Q80218672)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16955415%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

title

Long contiguous stretches of homozygosity in the human genome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16955415%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference

7

1 reference

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29 December 2019

14

Yuan-Tsong Chen

1 reference

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29 December 2019

author name string

Ling-Hui Li

1

1 reference

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29 December 2019

Sheng-Feng Ho

2

1 reference

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29 December 2019

Chien-Hsiun Chen

3

1 reference

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29 December 2019

Chun-Yu Wei

4

1 reference

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29 December 2019

Wan-Ching Wong

5

1 reference

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29 December 2019

Li-Ying Li

6

1 reference

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29 December 2019

Wen-Hung Chung

8

1 reference

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29 December 2019

Wen-Han Pan

9

1 reference

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29 December 2019

Ming-Ta M Lee

10

1 reference

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29 December 2019

Fuu-Jen Tsai

11

1 reference

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29 December 2019

Ching-Fen Chang

12

1 reference

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29 December 2019

Jer-Yuarn Wu

13

1 reference

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29 December 2019

publication date

1 November 2006

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29 December 2019

1 reference

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29 December 2019

volume

27

1 reference

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29 December 2019

page(s)

1115-1121

1 reference

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29 December 2019

issue

11

1 reference

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High-resolution analysis of DNA copy number using oligonucleotide microarrays

29 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Long homozygous chromosomal segments in reference families from the centre d'Etude du polymorphisme humain

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Medical genetics: a marker for Stevens-Johnson syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

The size distribution of homozygous segments in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

A high-resolution survey of deletion polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

The linkage disequilibrium maps of three human chromosomes across four populations reflect their demographic history and a common underlying recombination pattern

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

https://api.crossref.org/works/10.1002%2FHUMU.20399

1 reference

7 January 2021

The structure of haplotype blocks in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Extended tracts of homozygosity in outbred human populations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Whole-genome patterns of common DNA variation in three human populations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Common deletions and SNPs are in linkage disequilibrium in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Whole genome DNA copy number changes identified by high density oligonucleotide arrays

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Detection of large-scale variation in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Complex and segmental uniparental disomy (UPD): review and lessons from rare chromosomal complements

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Uniparental disomy (UPD) other than 15: phenotypes and bibliography updated.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Impact of parental relationships in maximum lod score affected sib-pair method

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Estimation of the inbreeding coefficient through use of genomic data

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Common deletion polymorphisms in the human genome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Pitfalls in homozygosity mapping.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Inversions with classical style and trendy lines

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Han Chinese cell and genome bank in Taiwan: purpose, design and ethical considerations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

MHC class I molecules and KIRs in human history, health and survival

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Large-scale copy number polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Fine-scale structural variation of the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Combinatorial pharmacogenetics

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

A new method for autozygosity mapping using single nucleotide polymorphisms (SNPs) and EXCLUDEAR.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20399

7 January 2021

Identifiers

DOI

10.1002/HUMU.20399

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16955415%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference