Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid (Q83171739)

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scientific article published on 19 April 2006

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English	Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid	scientific article published on 19 April 2006

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scholarly article

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19 January 2020

Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid (English)

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19 January 2020

12

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Norio Niikawa

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19 January 2020

Koh-ichiro Yoshiura

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Koh-ichiro Yoshiura

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19 January 2020

4

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Noriko Miyake

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19 January 2020

Nadiya Sosonkina

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Nadiya Sosonkina

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19 January 2020

Osamu Shimokawa

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Osamu Shimokawa

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19 January 2020

2

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Kiyonori Miura

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19 January 2020

Hideaki Masuzaki

3

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Hideaki Masuzaki

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19 January 2020

Shuichiro Yoshimura

10

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Shuichiro Yoshimura

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19 January 2020

Daisuke Nakayama

9

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Daisuke Nakayama

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19 January 2020

Tadayuki Ishimaru

13

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Tadayuki Ishimaru

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19 January 2020

author name string

Shoko Miura

1

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19 January 2020

Naoki Harada

7

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19 January 2020

Naomichi Matsumoto

11

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19 January 2020

publication date

19 April 2006

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19 January 2020

Journal of Human Genetics

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19 January 2020

51

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19 January 2020

5

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19 January 2020

412-417

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19 January 2020

https://scigraph.springernature.com/pub.10.1007/s10038-006-0376-7

0 references

BAC array CGH reveals genomic aberrations in idiopathic mental retardation.

1 reference

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Subtelomere specific microarray based comparative genomic hybridisation: a rapid detection system for cryptic rearrangements in idiopathic mental retardation

1 reference

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Fetal karyotyping after 28 weeks of gestation for late ultrasound findings in a low risk population

1 reference

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Genetic screening and diagnosis.

1 reference

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Microarray-based comparative genomic hybridization and its applications in human genetics

1 reference

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12 December 2020

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Detection of cell free placental DNA in maternal plasma: direct evidence from three cases of confined placental mosaicism

1 reference

https://pubmed.ncbi.nlm.nih.gov/16622586

12 December 2020

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Comparative genomic hybridization: a new tool for reproductive pathology

1 reference

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12 December 2020

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Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer

1 reference

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Genome-wide analysis of DNA copy-number changes using cDNA microarrays

1 reference

https://pubmed.ncbi.nlm.nih.gov/16622586

12 December 2020

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Microarray analysis of cell-free fetal DNA in amniotic fluid: a prenatal molecular karyotype.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16622586

12 December 2020

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Sonographic markers of fetal aneuploidy.

1 reference

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12 December 2020

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Large amounts of cell-free fetal DNA are present in amniotic fluid

1 reference

https://pubmed.ncbi.nlm.nih.gov/16622586

12 December 2020

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Fetal cells in the mother: from genetic diagnosis to diseases associated with fetal cell microchimerism

1 reference

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12 December 2020

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Prenatal diagnosis of trisomy 18: report of 30 cases

1 reference

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12 December 2020

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Analysis of uncultured amniocytes by comparative genomic hybridization: a prospective prenatal study

1 reference

https://pubmed.ncbi.nlm.nih.gov/16622586

12 December 2020

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Fetal cells and cell free fetal nucleic acids in maternal blood: new tools to study abnormal placentation?

1 reference

https://pubmed.ncbi.nlm.nih.gov/16622586

12 December 2020

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Fetomaternal cellular and plasma DNA trafficking: the Yin and the Yang

1 reference

https://pubmed.ncbi.nlm.nih.gov/16622586

12 December 2020

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CGH in the detection of confined placental mosaicism (CPM) in placentas of abnormal pregnancies

1 reference

https://pubmed.ncbi.nlm.nih.gov/16622586

12 December 2020

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High-resolution profiling of an 11 Mb segment of human chromosome 22 in sporadic schwannoma using array-CGH

1 reference

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12 December 2020

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Recent advances in fetal nucleic acids in maternal plasma

1 reference

https://pubmed.ncbi.nlm.nih.gov/16622586

12 December 2020

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Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16622586

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Fetal cell-free nucleic acids in the maternal circulation: new clinical applications

1 reference

https://pubmed.ncbi.nlm.nih.gov/16622586

12 December 2020

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Identifiers

10.1007/S10038-006-0376-7

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16622586%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16622586%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

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