(Q37803584)

23 August 2017

Behavioral features in young adults with FG syndrome (Opitz-Kaveggia syndrome). (English)

1 reference

23 August 2017

1 reference

John M Graham

1

1 reference

23 August 2017

Robin D Clark

series ordinal

2

1 reference

23 August 2017

John B Moeschler

series ordinal

3

1 reference

23 August 2017

R Curtis Rogers

series ordinal

4

1 reference

23 August 2017

1 November 2010

1 reference

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

23 August 2017

1 reference

23 August 2017

154C

1 reference

23 August 2017

477-485

1 reference

23 August 2017

4

1 reference

FG syndrome, an X-linked multiple congenital anomaly syndrome: the clinical phenotype and an algorithm for diagnostic testing

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2967396

Behavioral phenotype of sex chromosome aneuploidies: 48,XXYY, 48,XXXY, and 49,XXXXY

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2967396

A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2967396

Psychopharmacology in fragile X syndrome--present and future

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2967396

Clinical and behavioral characteristics in FG syndrome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2967396

Language and development in FG syndrome with callosal agenesis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2967396

Studies of malformation syndromes of man 33: the FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental retardation.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2967396

FG syndrome: report of three new families with linkage to Xq12-q22.1.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2967396

Behavior of 10 patients with FG syndrome (Opitz-Kaveggia syndrome) and the p.R961W mutation in the MED12 gene.

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2967396

Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndrome.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2967396

1 September 2018

Identifiers

DOI

10.1002/AJMG.C.30284

1 reference

23 August 2017

1 reference

23 August 2017

1 reference