Screening of SHOX gene sequence variants in Saudi Arabian children with idiopathic short stature.

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Screening of SHOX gene sequence variants in Saudi Arabian children with idiopathic short stature.

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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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Screening of SHOX gene sequenc ...... with idiopathic short stature.

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Screening of SHOX gene sequenc ...... with idiopathic short stature.

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label

Screening of SHOX gene sequenc ...... with idiopathic short stature.

@en

Screening of SHOX gene sequenc ...... with idiopathic short stature.

@nl

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Screening of SHOX gene sequenc ...... with idiopathic short stature.

@en

Screening of SHOX gene sequenc ...... with idiopathic short stature.

@nl

P1476

Screening of SHOX gene sequenc ...... with idiopathic short stature.

@en

P2093

Abdulla A Alharthi

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Ahmed Gaber

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Ehab I El-Hallous

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Hamed A Alghamdi

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Iman M Talaat

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Matar I Almalki

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P2860

A novel class of Pseudoautosomal region 1 deletions downstream of SHOX is associated with Leri-Weill dyschondrosteosis.

Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short stature

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

Leg length, body proportion, and health: a review with a note on beauty

Consanguinity among the Saudi Arabian population.

Identification of a major recombination hotspot in patients with short stature and SHOX deficiency.

SHOX haploinsufficiency and overdosage: impact of gonadal function status.

The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.

Prevalence of short stature in Saudi children and adolescents.

Phenotypic characterization of patients with deletions in the 3'-flanking SHOX region.

P304

327-332

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scholarly article

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10.3345/KJP.2017.60.10.327

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P433

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P478

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P577

2017-10-20T00:00:00Z

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29158767

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P932

5687980

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