Terminal deletion of chromosome 15q26.1: case report and brief literature review.
about
Insulin-like growth factors in embryonic and fetal growth and skeletal development (Review)Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delayMosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns-like phenotype.Array Characterization of Prenatally Diagnosed 15q26 Microdeletion and 2q37.1 Duplication: Report of a New Case with Multicystic Kidneys and Review of the Literature.Expanding the clinical spectrum of chromosome 15q26 terminal deletions associated with IGF-1 resistance.Short stature due to 15q26 microdeletion involving IGF1R: report of an additional case and review of the literature.
P2860
Terminal deletion of chromosome 15q26.1: case report and brief literature review.
description
2005 nî lūn-bûn
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2005年の論文
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2005年論文
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2005年論文
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2005年論文
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2005年論文
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2005年論文
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2005年论文
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2005年论文
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2005年论文
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name
Terminal deletion of chromosome 15q26.1: case report and brief literature review.
@ast
Terminal deletion of chromosome 15q26.1: case report and brief literature review.
@en
type
label
Terminal deletion of chromosome 15q26.1: case report and brief literature review.
@ast
Terminal deletion of chromosome 15q26.1: case report and brief literature review.
@en
prefLabel
Terminal deletion of chromosome 15q26.1: case report and brief literature review.
@ast
Terminal deletion of chromosome 15q26.1: case report and brief literature review.
@en
P2093
P2860
P356
P1476
Terminal deletion of chromosome 15q26.1: case report and brief literature review.
@en
P2093
Caraciolo J Fernandes
Joseph J Shen
Kushal Y Bhakta
Sarah J Marlin
P2860
P2888
P304
P356
10.1038/SJ.JP.7211301
P577
2005-06-01T00:00:00Z