about
A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseasesEffectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders.Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings.Emergency medical genomes: a breakthrough application of precision medicine.Renal systems biology of patients with systemic inflammatory response syndromeRapid whole genome sequencing and precision neonatologyWhole-Exome Sequencing and Whole-Genome Sequencing in Critically Ill Neonates Suspected to Have Single-Gene Disorders.
P50
Q34496202-0551EEBF-4F68-41CE-ACFA-E8A542B0905AQ34866575-720E4369-9289-423F-906D-75698924C3EAQ35776062-533C26A3-56F6-487E-BF3D-ECF077A44B63Q35903049-D86B1522-8D42-4BDC-AF1C-35619E354209Q36113202-C5B45F34-02A9-4491-8DBD-B991192A2020Q36315024-B008E044-3FA3-496F-AA32-03007D115691Q38673804-EDF2A960-886E-4BDB-86DF-D7CF642CD6C6
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Laurel Willig
@ast
Laurel Willig
@en
Laurel Willig
@es
Laurel Willig
@nl
Laurel Willig
@sl
type
label
Laurel Willig
@ast
Laurel Willig
@en
Laurel Willig
@es
Laurel Willig
@nl
Laurel Willig
@sl
prefLabel
Laurel Willig
@ast
Laurel Willig
@en
Laurel Willig
@es
Laurel Willig
@nl
Laurel Willig
@sl
P106
P31
P496
0000-0001-5780-418X