Short stature homeobox-containing gene duplications in 3.7% of girls with tall stature and normal karyotypes.

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Short stature homeobox-containing gene duplications in 3.7% of girls with tall stature and normal karyotypes.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Short stature homeobox-contain ...... stature and normal karyotypes.

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Short stature homeobox-contain ...... stature and normal karyotypes.

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Short stature homeobox-contain ...... stature and normal karyotypes.

@en

Short stature homeobox-contain ...... stature and normal karyotypes.

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Short stature homeobox-contain ...... stature and normal karyotypes.

@en

Short stature homeobox-contain ...... stature and normal karyotypes.

@nl

P1476

Short stature homeobox-contain ...... stature and normal karyotypes.

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P2093

Emmie N Upners

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Lise Aksglaede

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Morten Dunø

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Rikke B Jensen

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P2860

Crossover clustering and rapid decay of linkage disequilibrium in the Xp/Yp pseudoautosomal gene SHOX

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

Serum IGF1 and insulin levels in girls with normal and precocious puberty.

Defining the role of common variation in the genomic and biological architecture of adult human height.

Evaluation and phenotypic characteristics of 293 Danish girls with tall stature: effects of oral administration of natural 17β-estradiol.

Evaluation of SHOX copy number variations in patients with Müllerian aplasia.

Nationwide age references for sitting height, leg length, and sitting height/height ratio, and their diagnostic value for disproportionate growth disorders.

Turner syndrome presented with tall stature due to overdosage of the SHOX gene.

Skeletal overgrowth in transgenic mice that overexpress brain natriuretic peptide

Genotypes and phenotypes in children with short stature: clinical indicators of SHOX haploinsufficiency

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1651-1657

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scholarly article

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10.1111/APA.13969

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English

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106

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Anders Juul

Ewa Rajpert-De Meyts

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2017-07-01T00:00:00Z

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28667773

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P921

karyotype