(Q35694749)

9 August 2017

Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype (English)

1 reference

9 August 2017

0 references

6

Sabrina D Craigo

1 reference

9 August 2017

2

Diana W Bianchi

1 reference

9 August 2017

Linda Kleeman

1

1 reference

9 August 2017

Lisa G Shaffer

3

1 reference

9 August 2017

Emily Rorem

4

1 reference

9 August 2017

Janet Cowan

5

1 reference

9 August 2017

Hocine Tighiouart

7

1 reference

9 August 2017

Louise E Wilkins-Haug

8

1 reference

9 August 2017

1 December 2009

1 reference

9 August 2017

1 reference

9 August 2017

29

1 reference

9 August 2017

13

1 reference

9 August 2017

1213-1217

1 reference

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases

9 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4459708

Deletion 22q13.3 syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4459708

Microarray technology in obstetrics and gynecology: a guide for clinicians

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4459708

Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4459708

Telomeres: a diagnosis at the end of the chromosomes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4459708

Subtle chromosomal rearrangements in children with unexplained mental retardation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4459708

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4459708

Fetal ultrasound abnormalities: correlation with fetal karyotype, autopsy findings, and postnatal outcome--five-year prospective study

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4459708

Prenatal detection of subtelomeric rearrangements by multi-subtelomere FISH in a cohort of fetuses with major malformations.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4459708

Identification of a novel polymorphism--the duplication of the NPHP1 (nephronophthisis 1) gene.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4459708

Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4459708

Distribution of abnormal karyotypes among malformed fetuses detected by ultrasound throughout gestation

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19862770

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19862770

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/PD.2367

1 reference

9 August 2017

1 reference

9 August 2017

1 reference