Prenatal findings and delineation ofde novoconcurrent partial trisomy 7q(7q31.2 → qter) and partial monosomy 6q(6q26 → qter) by high-resolution array CGH (Q58029185)

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scientific article published on 01 November 2009

Language	Label	Description	Also known as
English	Prenatal findings and delineation ofde novoconcurrent partial trisomy 7q(7q31.2 → qter) and partial monosomy 6q(6q26 → qter) by high-resolution array CGH	scientific article published on 01 November 2009

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scholarly article

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12 February 2020

Prenatal findings and delineation of de novo concurrent partial trisomy 7q(7q31.2 --> qter) and partial monosomy 6q(6q26 --> qter) by high-resolution array CGH (English)

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12 February 2020

6

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12 February 2020

author name string

Kwong Wai Choy

1

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12 February 2020

Lin Wai Chan

2

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12 February 2020

Tak Yeung Leung

5

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12 February 2020

Mary H Y Tang

3

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12 February 2020

Lucy K L Ng

4

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12 February 2020

publication date

1 November 2009

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12 February 2020

Journal of Maternal-Fetal and Neonatal Medicine

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12 February 2020

22

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12 February 2020

11

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12 February 2020

1014-1020

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12 February 2020

Recurrent miscarriage

1 reference

https://api.crossref.org/works/10.3109%2F14767050902994812

21 January 2018

Duplication of 7q31.2----7qter and deficiency of 18qter: report of two patients and literature review

1 reference

https://api.crossref.org/works/10.3109%2F14767050902994812

21 January 2018

Partial trisomy for the long arm of chromosome 7. Case report and review

1 reference

https://api.crossref.org/works/10.3109%2F14767050902994812

21 January 2018

Clinical diagnosis of partial duplication 7q.

1 reference

https://api.crossref.org/works/10.3109%2F14767050902994812

21 January 2018

Prenatal diagnosis using interphase fluorescence in situ hybridization (FISH): 2-year multi-center retrospective study and review of the literature

1 reference

https://api.crossref.org/works/10.3109%2F14767050902994812

21 January 2018

Rapid and simple prenatal diagnosis of common chromosome disorders: advantages and disadvantages of the molecular methods FISH and QF-PCR.

1 reference

https://api.crossref.org/works/10.3109%2F14767050902994812

21 January 2018

Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

1 reference

https://api.crossref.org/works/10.3109%2F14767050902994812

21 January 2018

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

1 reference

https://api.crossref.org/works/10.3109%2F14767050902994812

21 January 2018

Detailed chromosomal and molecular genetic analysis of single cells by whole genome amplification and comparative genomic hybridisation

1 reference

https://api.crossref.org/works/10.3109%2F14767050902994812

21 January 2018

Prenatal detection of unbalanced chromosomal rearrangements by array CGH.

1 reference

https://api.crossref.org/works/10.3109%2F14767050902994812

21 January 2018

De novo 16p13.11 microdeletion identified by high-resolution array CGH in a fetus with increased nuchal translucency.

1 reference

https://api.crossref.org/works/10.3109%2F14767050902994812

21 January 2018

Pure partial trisomy 7q: two new patients and review

1 reference

https://api.crossref.org/works/10.3109%2F14767050902994812

21 January 2018

Molecular cytogenetic analysis and clinical findings in a newborn with prenatally diagnosed rec(7)dup(7q)inv(7)(p22q31.3)pat

1 reference

https://api.crossref.org/works/10.3109%2F14767050902994812

21 January 2018

Replication pattern of the X chromosomes in three X/autosomal translocations.

1 reference

https://api.crossref.org/works/10.3109%2F14767050902994812

21 January 2018

Chromosome 6q deletions: a report of two additional cases and a review of the literature

1 reference

https://api.crossref.org/works/10.3109%2F14767050902994812

21 January 2018

Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review.

1 reference

https://api.crossref.org/works/10.3109%2F14767050902994812

21 January 2018

Pre- and perinatal findings in partial trisomy 7q resulting from balanced parental translocations t(7;21) and t(4;7).

1 reference

https://api.crossref.org/works/10.3109%2F14767050902994812

21 January 2018

Identifiers

10.3109/14767050902994812

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19900039%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19900039%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

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