Implementation of an electronic genomic and family health history tool in primary prenatal care. (Q39234236)

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10 March 2020

title

Implementation of an electronic genomic and family health history tool in primary prenatal care (English)

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10 March 2020

6

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10 March 2020

Kevin S. Hughes

7

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10 March 2020

author name string

Emily A Edelman

1

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10 March 2020

Bruce K Lin

2

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10 March 2020

Teresa Doksum

3

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10 March 2020

Brian Drohan

4

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10 March 2020

Vaughn Edelson

5

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10 March 2020

James O'Leary

8

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10 March 2020

Shelley L Galvin

9

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10 March 2020

Nicole Degroat

10

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10 March 2020

Setul Pardanani

11

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10 March 2020

W Gregory Feero

12

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10 March 2020

Claire Adams

13

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10 March 2020

Renee Jones

14

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10 March 2020

Joan Scott

15

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10 March 2020

publication date

10 March 2014

1 reference

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American Journal of Medical Genetics Part C: Seminars in Medical Genetics

10 March 2020

published in

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10 March 2020

volume

166C

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10 March 2020

issue

1

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10 March 2020

page(s)

34-44

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ACOG Practice Bulletin No. 78: hemoglobinopathies in pregnancy

10 March 2020

cites work

1 reference

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ACOG Committee Opinion No. 442: Preconception and prenatal carrier screening for genetic diseases in individuals of Eastern European Jewish descent

21 January 2018

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21 January 2018

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21 January 2018

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Use of a web-based risk appraisal tool for assessing family history and lifestyle factors in primary care

21 January 2018

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Cystic fibrosis carrier screening in obstetric clinical practice: knowledge, practices, and barriers, a decade after publication of screening guidelines

21 January 2018

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Evaluation of a novel electronic genetic screening and clinical decision support tool in prenatal clinical settings

21 January 2018

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Practice parameter: screening and diagnosis of autism: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society

21 January 2018

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Evidence-based classification of recommendations on use of genomic tests in clinical practice: dealing with insufficient evidence

21 January 2018

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Guidelines for genetic risk assessment of hereditary breast and ovarian cancer: early disagreements and low utilization

21 January 2018

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Genetic counseling for fragile x syndrome: updated recommendations of the national society of genetic counselors

21 January 2018

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Clinical genetic evaluation of the child with mental retardation or developmental delays

21 January 2018

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Protocol for implementation of family health history collection and decision support into primary care using a computerized family health history system

21 January 2018

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Implementing family health history risk stratification in primary care: impact of guideline criteria on populations and resource demand

21 January 2018

1 reference

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Clinical utility of family history for cancer screening and referral in primary care: a report from the Family Healthware Impact Trial

21 January 2018

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A cancer genetics toolkit improves access to genetic services through documentation and use of the family history by primary-care clinicians

21 January 2018

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Fragile X syndrome: diagnostic and carrier testing

21 January 2018

1 reference

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