Cytogenetic and clinical studies in five cases of inv dup(15).
about
Autistic symptoms among children and young adults with isodicentric chromosome 15Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14.De novo partial trisomy 15q (proximal type).Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16An analysis of the parental age effect for inv dup (15).Inv dup(15) supernumerary marker chromosomes.Three probands with autistic disorder and isodicentric chromosome 15.Molecular cytogenetic evidence for a common breakpoint in the largest inverted duplications of chromosome 15.Chromosomal abnormalities and epilepsy: a review for clinicians and gene hunters.Discovery of supernumerary B chromosomes in Drosophila melanogasterCharacterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH).Extra structurally abnormal chromosomes (ESAC) detected at amniocentesis: frequency in approximately 75,000 prenatal cytogenetic diagnoses and associations with maternal and paternal ageIncidence and significance of supernumerary marker chromosomes in prenatal diagnosisMolecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNACytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients.Significant neuronal soma volume deficit in the limbic system in subjects with 15q11.2-q13 duplicationsDifferences between the pattern of developmental abnormalities in autism associated with duplications 15q11.2-q13 and idiopathic autism.Application of array-based comparative genomic hybridization to pediatric neurologic diseasesIntersitial deletion of 20p: new candidate region for Hirschsprung disease and autism?Inv dup (15) with mental retardation but few dysmorphic featuresAssociation analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder.Autism and maternally derived aberrations of chromosome 15q.A family with a grand-maternally derived interstitial duplication of proximal 15q.Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ hybridization.
P2860
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P2860
Cytogenetic and clinical studies in five cases of inv dup(15).
description
1979 nî lūn-bûn
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1979年の論文
@ja
1979年学术文章
@wuu
1979年学术文章
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1979年学术文章
@zh-cn
1979年学术文章
@zh-hans
1979年学术文章
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1979年学术文章
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1979年學術文章
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1979年學術文章
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name
Cytogenetic and clinical studies in five cases of inv dup
@nl
Cytogenetic and clinical studies in five cases of inv dup(15).
@en
type
label
Cytogenetic and clinical studies in five cases of inv dup
@nl
Cytogenetic and clinical studies in five cases of inv dup(15).
@en
prefLabel
Cytogenetic and clinical studies in five cases of inv dup
@nl
Cytogenetic and clinical studies in five cases of inv dup(15).
@en
P2093
P356
P1433
P1476
Cytogenetic and clinical studies in five cases of inv dup(15).
@en
P2093
J Heffelfinger
J V Higgins
L Wisniewski
P2888
P304
P356
10.1007/BF00399391
P577
1979-09-01T00:00:00Z