Newborn screening programs: should 22q11 deletion syndrome be added?

Newborn screening programs: should 22q11 deletion syndrome be added?

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http://www.wikidata.org/entity/Q37673851
Multiplex ligation-dependant probe amplification study of children with idiopathic mental retardation in South IndiaVariability in Clinical and Anatomical Manifestation of Velocardiofacial Syndrome Presents Diagnostic and Policy Uncertainty.Newborn screening for SCID in New York State: experience from the first two years.The 2nd Schizophrenia International Research Society Conference, 10-14 April 2010, Florence, Italy: summaries of oral sessions.Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome.Microdeletion and microduplication analysis of chinese conotruncal defects patients with targeted array comparative genomic hybridizationGenetics in schizophrenia: where are we and what next?Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndrome.A pyrosequencing-based assay for the rapid detection of the 22q11.2 deletion in DNA from buccal and dried blood spot samples.Assessment of parental disclosure of a 22q11.2 deletion syndrome diagnosis and implications for clinicians.Effort required to contact primary care providers after newborn screening identifies sickle cell trait.Screening newborns for primary T-cell immunodeficiencies: consensus and controversy.Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency.Genomic designation: how genetics can delineate new, phenotypically diffuse medical categories.
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Newborn screening programs: should 22q11 deletion syndrome be added?

Item
http://www.wikidata.org/entity/Q37673851
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on March 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Newborn screening programs: should 22q11 deletion syndrome be added?
@en
Newborn screening programs: should 22q11 deletion syndrome be added?
@nl
type
label
Newborn screening programs: should 22q11 deletion syndrome be added?
@en
Newborn screening programs: should 22q11 deletion syndrome be added?
@nl
prefLabel
Newborn screening programs: should 22q11 deletion syndrome be added?
@en
Newborn screening programs: should 22q11 deletion syndrome be added?
@nl
P1433
P1476
P2093
P2860
P2888
P304
P31
P356
P407
P433
P478
P577
P6179
P698
P356
P1433
P1476
Newborn screening programs: should 22q11 deletion syndrome be added?
@en
P2093
P2860
P2888
P304
P31
P356
10.1097/GIM.0B013E3181CDEB9A
P407
P433
P478
P577
P6179
P698