Familial 4.8 MB deletion on 18q23 associated with growth hormone insufficiency and phenotypic variability
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Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services.Interstitial de novo 18q22.3q23 deletion: clinical, neuroradiological and molecular characterization of a new case and review of the literatureA 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male miceEstablishing a reference group for distal 18q-: clinical description and molecular basis.Consequences of chromsome18q deletions.Adults with Chromosome 18 Abnormalities.Human ring chromosome registry for cases in the Chinese population: re-emphasizing Cytogenomic and clinical heterogeneity and reviewing diagnostic and treatment strategies.
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Familial 4.8 MB deletion on 18q23 associated with growth hormone insufficiency and phenotypic variability
description
im Februar 2012 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 02 February 2012
@en
wetenschappelijk artikel
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name
Familial 4.8 MB deletion on 18 ...... ncy and phenotypic variability
@en
Familial 4.8 MB deletion on 18 ...... ncy and phenotypic variability
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type
label
Familial 4.8 MB deletion on 18 ...... ncy and phenotypic variability
@en
Familial 4.8 MB deletion on 18 ...... ncy and phenotypic variability
@nl
prefLabel
Familial 4.8 MB deletion on 18 ...... ncy and phenotypic variability
@en
Familial 4.8 MB deletion on 18 ...... ncy and phenotypic variability
@nl
P2093
P2860
P50
P356
P1476
Familial 4.8 MB deletion on 18 ...... ncy and phenotypic variability
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P2093
Anna Soler
Carme Morales
Laia Rodríguez-Revenga
Núria Clusellas
Raquel Monné
P2860
P304
P356
10.1002/AJMG.A.34221
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P577
2012-02-02T00:00:00Z