Molecular basis for familial isolated growth hormone deficiency.
about
Characterization of the human growth hormone receptor gene and demonstration of a partial gene deletion in two patients with Laron-type dwarfismThe human growth hormone gene family: structure and evolution of the chromosomal locusA Chinese familial growth hormone deficiency with a deletion of 7.1 kb of DNAMolecular basis of human growth hormone gene deletions.Expression of the human growth hormone variant gene in cultured fibroblasts and transgenic mice.Analysis of human growth hormone gene 5' sequences in isolated growth hormone deficiency patientsDNA analysis in human diseaseShort stature--physiology and pathologyGenetics of isolated growth hormone deficiency.DNA restriction fragment analysis of the proopiomelanocortin gene in schizophrenia and bipolar disorders.Analysis of three restriction fragment length polymorphisms in the human type II procollagen gene.Molecular heterogeneity in the mild autosomal dominant forms of osteogenesis imperfecta.Use of molecular haplotypes specific for the human pro alpha 2(I) collagen gene in linkage analysis of the mild autosomal dominant forms of osteogenesis imperfecta.Utility and efficiency of linked marker genes for genetic counseling. III. Proportion of informative families under linkage disequilibriumGene conversions, deletions, and polymorphisms in congenital adrenal hyperplasia.Relative levels of methylation in human growth hormone and chorionic somatomammotropin genes in expressing and non-expressing tissuesGenetic Defects in the Growth Hormone-IGF-I Axis Causing Growth Hormone Insensitivity and Impaired Linear GrowthGenetic analysis of familial isolated growth hormone deficiency type I.Restriction fragment length polymorphism associated with the pro alpha 2(I) gene of human type I procollagen. Application to a family with an autosomal dominant form of osteogenesis imperfectaAnalysis of a break in chromosome 14 mapping to the region of the immunoglobulin heavy chain locusThe first intron of the human growth hormone gene contains a binding site for glucocorticoid receptor.Height matters-from monogenic disorders to normal variation.Dwarfs in art.The map of chromosome 20.Isolated growth hormone deficiency in two siblings because of paternal mosaicism for a mutation in the GH1 gene.Type IA isolated growth hormone deficiency (IGHD) consistent with compound heterozygous deletions of 6.7 and 7.6 Kb at the GH1 gene locus.Molecular study of human growth hormone gene cluster in three families with isolated growth hormone deficiency and similar phenotype
P2860
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P2860
Molecular basis for familial isolated growth hormone deficiency.
description
1981 nî lūn-bûn
@nan
1981年の論文
@ja
1981年学术文章
@wuu
1981年学术文章
@zh-cn
1981年学术文章
@zh-hans
1981年学术文章
@zh-my
1981年学术文章
@zh-sg
1981年學術文章
@yue
1981年學術文章
@zh
1981年學術文章
@zh-hant
name
Molecular basis for familial isolated growth hormone deficiency.
@ast
Molecular basis for familial isolated growth hormone deficiency.
@en
type
label
Molecular basis for familial isolated growth hormone deficiency.
@ast
Molecular basis for familial isolated growth hormone deficiency.
@en
prefLabel
Molecular basis for familial isolated growth hormone deficiency.
@ast
Molecular basis for familial isolated growth hormone deficiency.
@en
P2093
P2860
P356
P1476
Molecular basis for familial isolated growth hormone deficiency.
@en
P2093
B L Hjelle
J A Phillips
M Zachmann
P H Seeburg
P2860
P304
P356
10.1073/PNAS.78.10.6372
P407
P577
1981-10-01T00:00:00Z