Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center's Experience. (Q35910407)

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22 February 2020

title

Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center's Experience (English)

1 reference

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22 February 2020

6

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author name string

C Alexander Valencia

1

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22 February 2020

Ammar Husami

2

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22 February 2020

Jennifer Holle

3

1 reference

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22 February 2020

Judith A Johnson

4

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22 February 2020

Yaping Qian

5

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22 February 2020

Chao Wei

7

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22 February 2020

Subba Rao Indugula

8

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22 February 2020

Fanggeng Zou

9

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22 February 2020

Haiying Meng

10

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22 February 2020

Lijun Wang

11

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22 February 2020

Xia Li

12

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22 February 2020

Rachel Fisher

13

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22 February 2020

Tony Tan

14

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22 February 2020

Amber Hogart Begtrup

15

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22 February 2020

Kathleen Collins

16

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22 February 2020

Katie A Wusik

17

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22 February 2020

Derek Neilson

18

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22 February 2020

Thomas Burrow

19

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22 February 2020

Elizabeth Schorry

20

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22 February 2020

Robert Hopkin

21

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22 February 2020

Mehdi Keddache

22

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22 February 2020

John Barker Harley

23

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22 February 2020

Kenneth M Kaufman

24

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22 February 2020

Kejian Zhang

25

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22 February 2020

publication date

3 August 2015

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22 February 2020

published in

Frontiers in pediatrics

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22 February 2020

volume

3

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22 February 2020

page(s)

67

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Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings

22 February 2020

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24 September 2018

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PubMed

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inferred from PubMed ID database lookup

12 December 2020

based on heuristic

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007

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PubMed

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inferred from PubMed ID database lookup

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Identifiers

DOI

10.3389/FPED.2015.00067

1 reference

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22 February 2020

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22 February 2020

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