(Q50312865)

2 March 2018

title

Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family (English)

1 reference

2 March 2018

1 reference

phenotypic heterogeneity

1 reference

11

James F Gusella

1 reference

2 March 2018

Yihua Bao

10

object named as

Yihua Bao

1 reference

2 March 2018

author name string

Yiping Shen

1

1 reference

2 March 2018

Xiaoli Chen

2

1 reference

2 March 2018

Liwen Wang

3

1 reference

2 March 2018

Jin Guo

4

1 reference

2 March 2018

Jianliang Shen

5

1 reference

2 March 2018

Yu An

6

1 reference

2 March 2018

Haitao Zhu

7

1 reference

2 March 2018

Yanli Zhu

8

1 reference

2 March 2018

Ruolei Xin

9

1 reference

2 March 2018

Ting Zhang

12

1 reference

2 March 2018

Bai-Lin Wu

13

1 reference

2 March 2018

publication date

28 December 2010

1 reference

2 March 2018

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

published in

1 reference

2 March 2018

volume

156

1 reference

2 March 2018

issue

2

1 reference

2 March 2018

page(s)

225-232

1 reference

2 March 2018

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

Large, rare chromosomal deletions associated with severe early-onset obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

The association analysis of TBX6 polymorphism with susceptibility to congenital scoliosis in a Chinese Han population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

Comparative genomic hybridisation shows a partial de novo deletion 16p11.2 in a neonate with multiple congenital malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

Recurrent 16p11.2 microdeletions in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

Structural variation of chromosomes in autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

Duplication hotspots, rare genomic disorders, and common disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

Strong association of de novo copy number mutations with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

Microarray-based genomic DNA profiling technologies in clinical molecular diagnostics

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

A familial 593-kb microdeletion of 16p11.2 associated with mental retardation and hemivertebrae

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

Novel microdeletion syndromes detected by chromosome microarrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

Large recurrent microdeletions associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

Association between microdeletion and microduplication at 16p11.2 and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31147

21 January 2018

Identifiers

DOI

10.1002/AJMG.B.31147

1 reference

2 March 2018

1 reference

2 March 2018