(Q33676933)

28 July 2017

New autosomal recessive faciodigitogenital syndrome (English)

1 reference

autosomal recessive faciodigitogenital syndrome

28 July 2017

0 references

author name string

Teebi AS

1

1 reference

28 July 2017

Naguib KK

2

1 reference

28 July 2017

Al-Awadi S

3

1 reference

28 July 2017

Al-Saleh QA

4

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 June 1988

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

25

1 reference

28 July 2017

6

1 reference

28 July 2017

400-406

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050509

28 July 2017

1 reference

Aarskog's syndrome with Hirschsprung's disease, midgut malrotation, and dental anomalies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050509

Anomalous cerebral venous drainage in Aarskog syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050509

The Aarskog (facio-digital-genital) syndrome in South Africa. A report of three families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050509

Metatarsus adductus in two brothers with Aarskog syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050509

Autosomal dominant inheritance of the Aarskog syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050509

Hereditary contractures of the fingers (camptodactyly)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050509

A familial syndrome of short stature associated with facial dysplasia and genital anomalies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050509

Unusual facies, joint hypermobility, genital anomaly and short stature: a new dysmorphic syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050509

Osteochondritis dissecans with associated malformations in two brothers. A review of familial aspects

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050509

The facial-digital-genital (Aarskog) syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050509

The inheritance of the aarskog facial-digital-genital syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050509

Aarskog syndrome. New findings and genetic analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050509

21 June 2018

The Aarskog syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050509

Ophthalmic Manifestations of Aarskog (Facial-Digital-Genital) Syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050509

Aarskog syndrome: Significance for the surgeon

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050509

Aarskog syndrome with isolated growth hormone deficiency

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050509

[Aarskog's syndrome. Description of a case and endocrinological study]

30 October 2018

1 reference

12 December 2020

1 reference

12 December 2020

[Aarskog syndrome (author's transl)]

1 reference

12 December 2020

1 reference

12 December 2020

1 reference

12 December 2020

The Aarskog syndrome in a large family, suggestive for autosomal dominant inheritance

1 reference

12 December 2020

Aarskog syndrome: full male and female expression associated with an X-autosome translocation

1 reference

12 December 2020

Identifiers

PMCID

1050509

1 reference

28 July 2017

1 reference