FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15: II. Review of the literature.
about
Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative studyOrigins of accessory small ring marker chromosomes derived from chromosome 1.A supernumerary marker chromosome originating from two different regions of chromosome 18.Identification of supernumerary marker chromosomes derived from chromosomes 5, 6, 19, and 20 using FISH.Directly transmitted unbalanced chromosome abnormalities and euchromatic variantsComplex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among themMechanisms and consequences of small supernumerary marker chromosomes: from Barbara McClintock to modern genetic-counseling issues.Analphoid supernumerary marker chromosome characterized by aCGH and FISH as inv dup(3)(q25.33qter) de novo in a child with dysmorphic features and streaky pigmentation: case report.Identification of small marker chromosomes using microarray comparative genomic hybridization and multicolor fluorescent in situ hybridization.A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1-q12.1 in a healthy man.Somatic mosaicism in cases with small supernumerary marker chromosomes.Genome-wide construction of a series of designed segmental aneuploids in Saccharomyces cerevisiae.A case report of a meiotic segregation study on a small supernumerary marker chromosome.Small supernumerary marker chromosomes (sSMCs): a spotlight on some nomenclature problems.Molecular characterization of an analphoid supernumerary marker chromosome derived from 18q22.1➔qter in prenatal diagnosis: a case report.Tetrasomy 13q mosaicism associated with phylloid hypomelanosis and precocious puberty.Supernumerary marker chromosomes derived from chromosome 6: cytogenetic, molecular cytogenetic, and array CGH characterization.Non-chromosome 15 marker chromosome in a Prader-Willi syndrome patient with uniparental disomy
P2860
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P2860
FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15: II. Review of the literature.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
FISH and molecular studies of ...... II. Review of the literature.
@en
type
label
FISH and molecular studies of ...... II. Review of the literature.
@en
prefLabel
FISH and molecular studies of ...... II. Review of the literature.
@en
P1476
FISH and molecular studies of ...... II. Review of the literature.
@en
P2093
P304
P356
10.1002/(SICI)1096-8628(19980203)75:4<367::AID-AJMG5>3.3.CO;2-O
P577
1998-02-01T00:00:00Z