The 22q11.2 deletion in African-American patients: an underdiagnosed population? - Wikidata - wikimedia - TriplyDB

The 22q11.2 deletion in African-American patients: an underdiagnosed population?

The 22q11.2 deletion in African-American patients: an underdiagnosed population?

http://www.wikidata.org/entity/Q54918709

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Evidence for association of hyperprolinemia with schizophrenia and a measure of clinical outcome Primary immunodeficiency diagnosed at autopsy: a case report Characteristic face: a key indicator for direct diagnosis of 22q11.2 deletions in Chinese velocardiofacial syndrome patients.Psychiatric disorders in 22q11.2 deletion syndrome are prevalent but undertreated.Atypical face shape and genomic structural variants in epilepsy.22q11.2 deletion syndrome Developmental trajectories in 22q11.2 deletion.How to diagnose the 22q11.2 deletion syndrome in patients with schizophrenia: a case report Newborn screening programs: should 22q11 deletion syndrome be added?Asymmetric crying facies in the 22q11.2 deletion syndrome: implications for future screening.The benefits and limitations of cell-free DNA screening for 22q11.2 deletion syndrome.Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator.22q11 deletion syndrome: is that what they used to call . . . ?IQ and hemizygosity for the Val158 Met functional polymorphism of COMT in 22q11DS.Dental treatment of a patient with Opitz G/BBB syndrome.22q11.2 deletion syndrome in diverse populations.Orthopaedic manifestations within the 22q11.2 Deletion syndrome: A systematic review.Sclerocornea associated with the chromosome 22q11.2 deletion syndrome.The Psychosis Spectrum in 22q11.2 Deletion Syndrome Is Comparable to That of Nondeleted Youths.

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P2860

The 22q11.2 deletion in African-American patients: an underdiagnosed population?

http://www.wikidata.org/entity/Q54918709

description

2005 nî lūn-bûn

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

@zh-my

2005年学术文章

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2005年學術文章

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2005年學術文章

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name

The 22q11.2 deletion in African-American patients: an underdiagnosed population?

@en

The 22q11.2 deletion in African-American patients: an underdiagnosed population?

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type

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The 22q11.2 deletion in African-American patients: an underdiagnosed population?

@en

The 22q11.2 deletion in African-American patients: an underdiagnosed population?

@nl

prefLabel

The 22q11.2 deletion in African-American patients: an underdiagnosed population?

@en

The 22q11.2 deletion in African-American patients: an underdiagnosed population?

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P1433

American Journal of Medical Genetics

P1476

The 22q11.2 deletion in African-American patients: an underdiagnosed population?

@en

P2093

Abbas Jawad

http://www.w3.org/2001/XMLSchema#string

Beverly S Emanuel

http://www.w3.org/2001/XMLSchema#string

Deborah Driscoll

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Don Larossa

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Elaine H Zackai

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Elizabeth Goldmuntz

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Jason R Catanzaro

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Melissa K Tonnesen

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Nancy Minugh-Purvis

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Richard E Kirschner

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P2860

The Philadelphia story: the 22q11.2 deletion: report on 250 patients

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11

Chromosome 22q11.2 deletion in a boy with Opitz (G/BBB) syndrome.

Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis

A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome.

Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.

Neural tube defects and deletions of 22q11.

Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.

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242-246

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scholarly article

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10.1002/AJMG.A.30069

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3

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134

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Donna M McDonald-McGinn

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2005-04-01T00:00:00Z

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7980575

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15754359

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2810968

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