IGF1R Gene Alterations in Small for Gestational Age (SGA) Children.

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IGF1R Gene Alterations in Small for Gestational Age (SGA) Children.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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IGF1R Gene Alterations in Small for Gestational Age (SGA) Children.

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IGF1R Gene Alterations in Small for Gestational Age

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IGF1R Gene Alterations in Small for Gestational Age (SGA) Children.

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IGF1R Gene Alterations in Small for Gestational Age

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IGF1R Gene Alterations in Small for Gestational Age (SGA) Children.

@en

IGF1R Gene Alterations in Small for Gestational Age

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P1476

IGF1R Gene Alterations in Small for Gestational Age (SGA) Children.

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P2093

Aleksandar Dimovski

http://www.w3.org/2001/XMLSchema#string

Aleksandra Janchevska

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Kristina Mironska

http://www.w3.org/2001/XMLSchema#string

Velibor Tasic

http://www.w3.org/2001/XMLSchema#string

Zoran Gucev

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P2860

A heterozygous mutation of the insulin-like growth factor-I receptor causes retention of the nascent protein in the endoplasmic reticulum and results in intrauterine and postnatal growth retardation.

Insulin-like growth factor I receptor primary structure: comparison with insulin receptor suggests structural determinants that define functional specificity

International Small for Gestational Age Advisory Board consensus development conference statement: management of short children born small for gestational age, April 24-October 1, 2001.

Genetic factors associated with small for gestational age birth and the use of human growth hormone in treating the disorder.

The insulin-like growth factor system and fetal growth restrictionn.

Familial short stature with IGF-I receptor gene anomaly.

A novel heterozygous IGF-1 receptor mutation associated with hypoglycemia.

Response to Growth Hormone Treatment in a Patient with Insulin-like Growth Factor 1 Receptor (IGF1R) Deletion.

A variable degree of intrauterine and postnatal growth retardation in a family with a missense mutation in the insulin-like growth factor I receptor.

Three novel IGF1R mutations in microcephalic patients with prenatal and postnatal growth impairment.

P304

790-793

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P31

scholarly article

P356

10.3889/OAMJMS.2018.209

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P433

http://www.w3.org/2001/XMLSchema#string

P478

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P577

2018-05-01T00:00:00Z

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P698

29896311

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P932

5985885

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