Karyotype versus microarray testing for genetic abnormalities after stillbirth (Q34966044)

5 August 2017

title

Karyotype versus microarray testing for genetic abnormalities after stillbirth (English)

1 reference

5 August 2017

0 references

0 references

Robert L Goldenberg

1 reference

5 August 2017

Uma M Reddy

1 reference

5 August 2017

Michael W Varner

0 references

Marian Willinger

1 reference

5 August 2017

Robert M Silver

1 reference

5 August 2017

Halit Pinar

1 reference

5 August 2017

Josefine Heim-Hall

1 reference

5 August 2017

Ronald J Wapner

1 reference

5 August 2017

Donald J Dudley

1 reference

5 August 2017

George R Saade

1 reference

5 August 2017

Radek Bukowski

1 reference

5 August 2017

Vanessa R Thorsten

1 reference

5 August 2017

Corette B Parker

1 reference

5 August 2017

Grier P Page

1 reference

5 August 2017

Carolyn D Drews-Botsch

1 reference

5 August 2017

Brynn Levy

1 reference

5 August 2017

Barbara J Stoll

1 reference

5 August 2017

Barbara M O'Brien

1 reference

5 August 2017

NICHD Stillbirth Collaborative Research Network

series ordinal

1 reference

5 August 2017

language of work or name

English

0 references

publication date

1 December 2012

1 reference

The New England Journal of Medicine

5 August 2017

published in

1 reference

5 August 2017

volume

367

1 reference

5 August 2017

1 reference

5 August 2017

page(s)

2185-2193

1 reference

Chromosomal microarray versus karyotyping for prenatal diagnosis

5 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Phenotypic heterogeneity of genomic disorders and rare copy-number variants

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Causes of death among stillbirths

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Stillbirth Collaborative Research Network: design, methods and recruitment experience

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

The stillbirth collaborative research network postmortem examination protocol

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Copy-number changes in prenatal diagnosis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Genome-wide array-based copy number profiling in human placentas from unexplained stillbirths

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

The Stillbirth Collaborative Research Network (SCRN) placental and umbilical cord examination protocol

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Microduplication 22q11.2: a new chromosomal syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Confidence intervals for a ratio of binomial proportions based on paired data

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Wisconsin Stillbirth Service Program: I. Establishment and assessment of a community-based program for etiologic investigation of intrauterine deaths

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Diagnostic exome sequencing in persons with severe intellectual disability

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Array comparative genomic hybridization for genetic evaluation of fetal loss between 10 and 20 weeks of gestation

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Fetal and perinatal mortality, United States, 2005.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Cytogenetic analysis after evaluation of 750 fetal deaths: proposal for diagnostic workup

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to grow in vitro.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4295117

Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net!

26 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23215556

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The intrafamilial variability of the 22q11.2 microduplication encompasses a spectrum from minor cognitive deficits to severe congenital anomalies

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23215556

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Array-based comparative genomic hybridization (aCGH) in the genetic evaluation of stillbirth

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23215556

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1056/NEJMOA1201569

1 reference

5 August 2017

1 reference

5 August 2017

1 reference