(Q38567069)

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Reproductive genetic counseling challenges associated with diagnostic exome sequencing in a large academic private reproductive genetic counseling practice

scientific article published on 15 August 2015

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scholarly article

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Europe PubMed Central

4 September 2017

Reproductive genetic counseling challenges associated with diagnostic exome sequencing in a large academic private reproductive genetic counseling practice (English)

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Europe PubMed Central

4 September 2017

Christine M. Eng

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object named as

Christine M Eng

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Europe PubMed Central

4 September 2017

author name string

Lauren E Westerfield

1

1 reference

Europe PubMed Central

4 September 2017

Samantha R Stover

2

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Europe PubMed Central

4 September 2017

Veena S Mathur

3

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Europe PubMed Central

4 September 2017

Salma A Nassef

4

1 reference

Europe PubMed Central

4 September 2017

Tiffiney G Carter

5

1 reference

Europe PubMed Central

4 September 2017

Yaping Yang

6

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Europe PubMed Central

4 September 2017

Ignatia B Van den Veyver

8

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Europe PubMed Central

4 September 2017

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publication date

15 August 2015

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Europe PubMed Central

4 September 2017

Prenatal Diagnosis

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Europe PubMed Central

4 September 2017

35

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Europe PubMed Central

4 September 2017

10

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Europe PubMed Central

4 September 2017

1022-1029

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Europe PubMed Central

4 September 2017

Including prenatal diagnoses in birth defects monitoring: Experience of the Metropolitan Atlanta Congenital Defects Program.

1 reference

https://api.crossref.org/works/10.1002%2FPD.4674

21 January 2018

Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis

1 reference

https://api.crossref.org/works/10.1002%2FPD.4674

21 January 2018

Genetic assessment following increased nuchal translucency and normal karyotype.

1 reference

https://api.crossref.org/works/10.1002%2FPD.4674

21 January 2018

Increased nuchal translucency in the presence of normal chromosomes: what's next?

1 reference

https://api.crossref.org/works/10.1002%2FPD.4674

21 January 2018

Molecular findings among patients referred for clinical whole-exome sequencing

1 reference

https://api.crossref.org/works/10.1002%2FPD.4674

21 January 2018

Clinical whole-exome sequencing for the diagnosis of mendelian disorders

1 reference

https://api.crossref.org/works/10.1002%2FPD.4674

21 January 2018

Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes

1 reference

https://api.crossref.org/works/10.1002%2FPD.4674

21 January 2018

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

1 reference

https://api.crossref.org/works/10.1002%2FPD.4674

21 January 2018

Guidelines for return of research results from pediatric genomic studies: deliberations of the Boston Children's Hospital Gene Partnership Informed Cohort Oversight Board

1 reference

https://api.crossref.org/works/10.1002%2FPD.4674

21 January 2018

Clinical diagnosis by whole-genome sequencing of a prenatal sample

1 reference

https://api.crossref.org/works/10.1002%2FPD.4674

21 January 2018

Exome sequencing improves genetic diagnosis of structural fetal abnormalities revealed by ultrasound

1 reference

https://api.crossref.org/works/10.1002%2FPD.4674

21 January 2018

Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype.

1 reference

https://api.crossref.org/works/10.1002%2FPD.4674

21 January 2018

Exome sequencing for gene discovery in lethal fetal disorders--harnessing the value of extreme phenotypes

1 reference

https://api.crossref.org/works/10.1002%2FPD.4674

21 January 2018

ACMG clinical laboratory standards for next-generation sequencing

1 reference

https://api.crossref.org/works/10.1002%2FPD.4674

21 January 2018

Genetic counselors' views and experiences with the clinical integration of genome sequencing

1 reference

https://api.crossref.org/works/10.1002%2FPD.4674

21 January 2018

Identifiers

10.1002/PD.4674

1 reference

Europe PubMed Central

4 September 2017

1 reference

Europe PubMed Central

4 September 2017

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