(Q33537397)

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Townes-Brocks syndrome

scientific article

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scholarly article

1 reference

Europe PubMed Central

27 July 2017

1 reference

Europe PubMed Central

Townes-Brocks syndrome. (English)

1 reference

Europe PubMed Central

27 July 2017

author name string

Powell CM

1

1 reference

Europe PubMed Central

27 July 2017

Michaelis RC

2

1 reference

Europe PubMed Central

27 July 2017

language of work or name

0 references

publication date

1 February 1999

1 reference

Europe PubMed Central

27 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

27 July 2017

36

1 reference

Europe PubMed Central

27 July 2017

2

1 reference

Europe PubMed Central

27 July 2017

89-93

1 reference

Europe PubMed Central

27 July 2017

Townes-Brocks and Pendred syndrome in the same patient.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

14 July 2018

Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

14 July 2018

Isolation, characterization, and organ-specific expression of two novel human zinc finger genes related to the Drosophila gene spalt

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

14 July 2018

The need for more accurate and timely diagnosis in Fanconi anemia: a report from the International Fanconi Anemia Registry.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

14 July 2018

Description of a patient with difficult nosological classification: Goldenhar syndrome or Townes-Brocks syndrome?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

14 July 2018

Spectrum of anomalies in Fanconi anaemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

14 July 2018

Hereditary syndrome of imperforate anus with hand, foot, and ear anomalies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

14 July 2018

A new polydactyly/imperforate-anus/vertebral-anomalies syndrome?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

14 July 2018

Townes syndrome. A distinct multiple malformation syndrome resembling VACTERL association.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

14 July 2018

A new family with the Townes-Brocks syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

14 July 2018

VACTERL with hydrocephalus: further delineation of the syndrome(s)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

14 July 2018

Townes-Brocks syndrome. Report of a case and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

14 July 2018

The Townes-Brocks syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

14 July 2018

Townes-Brocks syndrome in two mentally retarded youngsters.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

14 July 2018

Townes-Brocks syndrome. Case report and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

14 July 2018

Familial anal abnormality

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

14 July 2018

Autosomal dominant transmission of a syndrome of anal, ear, renal, and radial congenital malformations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

14 July 2018

Townes-Brocks syndrome associated with mental retardation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

31 October 2018

Townes-Brocks syndrome in an infant with translocation t (5;16).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

31 October 2018

Hearing loss in Townes-Brocks syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

31 October 2018

Syndrome of imperforate anus, abnormalities of hands and feet, satyr ears, and sensorineural deafness.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

31 October 2018

The Holt-Oram syndrome with previously undescribed associated anomalies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

31 October 2018

Limb anomalies in DiGeorge and CHARGE syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

31 October 2018

Upper limb malformations in DiGeorge syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734298

31 October 2018

Familial occurrence of hemifacial microsomia with radial limb defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/10051003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypic variability in Townes-Brocks syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/10051003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Townes-Brocks syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/10051003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

VACTERL with hydrocephalus: one end of the Fanconi anemia spectrum of anomalies?

1 reference

https://pubmed.ncbi.nlm.nih.gov/10051003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

VACTERL with hydrocephalus: spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance

1 reference

https://pubmed.ncbi.nlm.nih.gov/10051003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PHAVER syndrome: an autosomal recessive syndrome of limb pterygia, congenital heart anomalies, vertebral defects, ear anomalies, and radial defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/10051003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Clinical heterogeneity of Townes-Brocks syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/10051003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three-generation family with resemblance to Townes-Brocks syndrome and Goldenhar/oculoauriculovertebral spectrum

1 reference

https://pubmed.ncbi.nlm.nih.gov/10051003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[The Townes-Brocks syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/10051003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Townes-Brocks syndrome presenting as end stage renal failure

1 reference

https://pubmed.ncbi.nlm.nih.gov/10051003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

27 July 2017

1 reference

Europe PubMed Central

27 July 2017

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