Further evidence for deletions in 7p14.1 contributing to nonsyndromic cleft lip with or without cleft palate.

about

Genome-Wide Association of Copy Number Polymorphisms and Kidney Function.Identification of Isthmin 1 as a Novel Clefting and Craniofacial Patterning Gene in Humans.Copy Number Changes Identified Using Whole Exome Sequencing in Nonsyndromic Cleft Lip and Palate in a Honduran Population.

P2860

Q36263854-38FA781F-94C6-41F7-B24E-E3A7255E8F9E Q49834334-9986196C-D7FF-40FA-BF57-A8E6FB63AC8C Q55154999-7CB04DFA-D7DB-44E3-8899-43E541EDDFD7

P2860

Further evidence for deletions in 7p14.1 contributing to nonsyndromic cleft lip with or without cleft palate.

Item

http://www.wikidata.org/entity/Q39626740

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Further evidence for deletions ...... with or without cleft palate.

@en

Further evidence for deletions ...... with or without cleft palate.

@nl

type

Item

label

Further evidence for deletions ...... with or without cleft palate.

@en

Further evidence for deletions ...... with or without cleft palate.

@nl

prefLabel

Further evidence for deletions ...... with or without cleft palate.

@en

Further evidence for deletions ...... with or without cleft palate.

@nl

P1476

Further evidence for deletions ...... with or without cleft palate.

@en

P2093

Alexander Hemprich

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

Alexander M Zink

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

Andrea Hofmann

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

Ann-Kathrin Hoebel

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

Anne C Böhmer

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

Elisabeth Mangold

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

Gül Schmidt

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

Jessica Becker

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

Johanna Klamt

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

Kerstin U Ludwig

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

P2860

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Detection of large-scale variation in the human genome

A copy number variation map of the human genome

Large-scale copy number polymorphism in the human genome

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci

A copy number variation morbidity map of developmental delay

Fine tuning of craniofacial morphology by distant-acting enhancers

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

P304

767-772

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

P31

scholarly article

P356

10.1002/BDRA.23539

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

P433

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

P478

106

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

P50

Franziska Degenhardt

Markus Martini

P577

2016-07-07T00:00:00Z

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

P698

27384521

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

Further evidence for deletions in 7p14.1 contributing to nonsyndromic cleft lip with or without cleft palate.

about

P2860

P2860

Further evidence for deletions in 7p14.1 contributing to nonsyndromic cleft lip with or without cleft palate.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698