(Q57279132)

8

object named as

Latha Soorya

0 references

Ana Tryfon

6

object named as

Ana Tryfon

0 references

author name string

Tracy Brandt

1

0 references

Khyati Desai

2

0 references

David Grodberg

3

0 references

Lakshmi Mehta

4

0 references

Ninette Cohen

5

0 references

Alexander Kolevzon

7

0 references

Lisa Edelmann

American Journal of Medical Genetics

10

0 references

language of work or name

English

0 references

publication date

4 April 2012

0 references

published in

0 references

volume

158A

0 references

issue

5

0 references

page(s)

1170-1177

0 references

cites work

Advances in autism genetics: on the threshold of a new neurobiology

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Transcriptional control of axonal guidance and sorting in dorsal interneurons by the Lim-HD proteins Lhx9 and Lhx1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: the Special Needs and Autism Project (SNAP)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Clinical spectrum associated with hepatocyte nuclear factor-1beta mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Pervasive developmental disorders in preschool children: confirmation of high prevalence

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Detection of large-scale variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Recurrent aberrations identified by array-CGH in patients with Mayer-Rokitansky-Küster-Hauser syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Copy number gain at Xp22.31 includes complex duplication rearrangements and recurrent triplications.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Autism in three patients with cystic or hyperechogenic kidneys and chromosome 17q12 deletion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Structural variation of chromosomes in autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Private inherited microdeletion/microduplications: implications in clinical practice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Autistic disorder and 22q11.2 duplication.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Microduplication 22q11.2 in a child with autism spectrum disorder: clinical and genetic study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Strong association of de novo copy number mutations with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267

LIM-homeodomain proteins Lhx1 and Lhx5, and their cofactor Ldb1, control Purkinje cell differentiation in the developing cerebellum

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35267