Hereditary hearing loss SNP-microarray pilot study.

about

Hereditary hearing loss SNP-microarray pilot study.

Item

http://www.wikidata.org/entity/Q55436692

description

2018 nî lūn-bûn

@nan

2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

@zh

2018年學術文章

@zh-hant

name

Hereditary hearing loss SNP-microarray pilot study.

@en

Hereditary hearing loss SNP-microarray pilot study.

@nl

type

Item

label

Hereditary hearing loss SNP-microarray pilot study.

@en

Hereditary hearing loss SNP-microarray pilot study.

@nl

prefLabel

Hereditary hearing loss SNP-microarray pilot study.

@en

Hereditary hearing loss SNP-microarray pilot study.

@nl

P1476

Hereditary hearing loss SNP-microarray pilot study.

@en

P2093

Indrajit Nanda

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

Jörg Schröder

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

Michaela A H Hofrichter

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

Thomas Haaf

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

Wafaa Shehata-Dieler

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

P2860

Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment

Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concerns

Identification of copy number variants through whole-exome sequencing in autosomal recessive nonsyndromic hearing loss.

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data.

Copy number variants are a common cause of non-syndromic hearing loss

Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature.

Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations.

Disruption of the ATE1 and SLC12A1 Genes by Balanced Translocation in a Boy with Non-Syndromic Hearing Loss.

Non-syndromic hearing loss gene identification: A brief history and glimpse into the future.

Navigating genetic diagnostics in patients with hearing loss.

P2888

s13104-018-3466-7

P304

391

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

P31

scholarly article

P356

10.1186/S13104-018-3466-7

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

P433

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

P478

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

P50

Barbara Vona

P577

2018-06-14T00:00:00Z

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

P6179

1104600405

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

P698

29903040

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

P932

6003021

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