Genetic linkage of human height is confirmed to 9q22 and Xq24. (Q47351324)

14 January 2018

title

Genetic linkage of human height is confirmed to 9q22 and Xq24. (English)

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14 January 2018

Hong-Wen Deng

13

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author name string

Yao-Zhong Liu

1

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Peng Xiao

2

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Yan-fang Guo

3

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Dong-Hai Xiong

4

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Lan-Juan Zhao

5

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Hui Shen

6

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14 January 2018

Yong-Jun Liu

7

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Volodymyr Dvornyk

8

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Ji-Rong Long

9

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Hong-Yi Deng

10

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Jin-Long Li

11

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Robert R Recker

12

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publication date

31 January 2006

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14 January 2018

published in

Human Genetics

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14 January 2018

volume

119

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issue

3

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page(s)

295-304

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14 January 2018

A cross-sectional examination of height, weight, and body mass index in adult twins

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00439-006-0136-Y

Genome scan for body mass index and height in the Framingham Heart Study

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Parametric and nonparametric linkage analysis: a unified multipoint approach

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A whole-genome linkage scan suggests several genomic regions potentially containing QTLs underlying the variation of stature

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A major gene model of adult height is suggested in Chinese

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QTLs for height: results of a full genome scan in Dutch sibling pairs

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Quantitative genetic analysis of longitudinal trends in height: preliminary results from the Louisville Twin Study.

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X-linked mental retardation with isolated growth hormone deficiency is mapped to Xq22-Xq27.2 in one family

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Genetic Dissection of Human Stature in a Large Sample of Multiplex Pedigrees

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Major gene control of human body height, weight and BMI in five ethnically different populations

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Collagen Ialpha1 Sp1 polymorphism, bone mass, and bone turnover in healthy French premenopausal women: the OFELY study

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Problems in the definition, interpretation, and evaluation of genetic heterogeneity

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Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height

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Major recessive gene(s) with considerable residual polygenic effect regulating adult height: confirmation of genomewide scan results for chromosomes 6, 9, and 12.

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Nonreplication in genetic studies of complex diseases--lessons learned from studies of osteoporosis and tentative remedies

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Familial X-linked mental retardation and isolated growth hormone deficiency: clinical and molecular findings

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Identification of novel human GH-1 gene polymorphisms that are associated with growth hormone secretion and height

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Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure

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Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups

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Toward high-throughput genotyping: dynamic and automatic software for manipulating large-scale genotype data using fluorescently labeled dinucleotide markers

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Novel X-linked mental retardation syndrome with short stature maps to Xq24.

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Robust variance-components approach for assessing genetic linkage in pedigrees

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Target height as predicted by parental heights in a population-based study

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Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2.

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TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS

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Ror2, encoding a receptor-like tyrosine kinase, is required for cartilage and growth plate development

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Evidence for linkage of stature to chromosome 3p26 in a large U.K. Family data set ascertained for type 2 diabetes

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Multipoint quantitative-trait linkage analysis in general pedigrees

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A male-specific quantitative trait locus on 1p21 controlling human stature

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One gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B.

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Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

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Age-stratified QTL genome scan analyses for anthropometric measures

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Assessing genetic linkage and association with robust components of variance approaches

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A new X linked mental retardation (XLMR) syndrome with short stature, small testes, muscle wasting, and tremor localises to Xq24-q25.

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Combined analysis of genomewide scans for adult height: results from the NHLBI Family Blood Pressure Program

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10.1007/S00439-006-0136-Y

Identifiers

DOI

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14 January 2018

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14 January 2018