Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity? - Wikidata - awgldk - TriplyDB

Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?

Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?

http://www.wikidata.org/entity/Q36645370

about

Small supernumerary marker chromosomes and their correlation with specific syndromes Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011 Centromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogenetics.The clinical analysis of small supernumerary marker chromosomes in 17 children with mos 45,X/46,X,+mar karyotype.Small supernumerary marker chromosomes and uniparental disomy have a story to tell Chromosomal mosaicism goes global.Handling small supernumerary marker chromosomes in prenatal diagnostics.Marker chromosomes.Complex small supernumerary marker chromosome with a 15q/16p duplication: clinical implications.Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22- A Case Report.Molecular characterization of 20 small supernumerary marker chromosome cases using array comparative genomic hybridization and fluorescence in situ hybridization.Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosis Complex small supernumerary marker chromosomes - an update Characterizing small supernumerary marker chromosomes with combination of multiple techniques.Partial trisomy 1q41-qter and partial trisomy 9pter-9q21.32 in a newborn infant: an array CGH analysis and review.

P2860

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P2860

Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?

http://www.wikidata.org/entity/Q36645370

description

2008 nî lūn-bûn

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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2008年论文

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2008年论文

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name

Complex rearranged small super ...... for an underestimated entity?

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Complex rearranged small super ...... for an underestimated entity?

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Complex rearranged small super ...... for an underestimated entity?

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Complex rearranged small super ...... for an underestimated entity?

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Complex rearranged small super ...... for an underestimated entity?

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Complex rearranged small super ...... for an underestimated entity?

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Molecular Cytogenetics

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Complex rearranged small super ...... for an underestimated entity?

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P2093

Adayapalam Nandini

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Anja Weise

http://www.w3.org/2001/XMLSchema#string

Daniela Reich

http://www.w3.org/2001/XMLSchema#string

Elisabeth Ewers

http://www.w3.org/2001/XMLSchema#string

Franz Binkert

http://www.w3.org/2001/XMLSchema#string

Hasmik Mkrtchyan

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Jasen Anderson

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Laura Rodriguez

http://www.w3.org/2001/XMLSchema#string

Madeleine Gross

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Nadezda Kosyakova

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P2860

De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints

Microdissection based high resolution multicolor banding for all 24 human chromosomes.

Cytogenetic analysis by chromosome painting using DOP-PCR amplified flow-sorted chromosomes.

Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations

Small supernumerary marker chromosomes (sSMC) in humans.

Array painting using microdissected chromosomes to map chromosomal breakpoints.

A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH).

Detailed characterization of 12 supernumerary ring chromosomes using micro-FISH and search for uniparental disomy.

FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15: II. Review of the literature.

Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements.

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scholarly article

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10.1186/1755-8166-1-6

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1

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2008-04-15T00:00:00Z

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5265980

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1030033660

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18471318

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2375881

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