(Q28769838)

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Triphalangeal thumb

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

1 reference

Europe PubMed Central

Triphalangeal thumb (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

0 references

author name string

Qazi Q

1

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

Kassner EG

2

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

language of work or name

0 references

publication date

1 August 1988

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

25

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

505-520

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

Familial heart disease with skeletal malformations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

16 March 2017

Congenital (erythroid) hypoplastic anemia. A 25-year study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

16 March 2017

The insertions of the flexores pollicis longus et digitorum profundus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

20 June 2018

The IVIC syndrome: a new autosomal dominant complex pleiotropic syndrome with radial ray hypoplasia, hearing impairment, external ophthalmoplegia, and thrombocytopenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

20 June 2018

Hypomelanosis of Ito with triphalangeal thumbs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

20 June 2018

An autosomal dominant syndrome of radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

20 June 2018

The Langer-Giedion phenotype associated with a unique skeletal finding in a mentally retarded adolescent male. A case report.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

20 June 2018

Abnormal distal phalanges and nails, deafness, mental retardation, and seizure disorder: a new familial syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

20 June 2018

Congenital anemia and triphalangeal thumbs: A new syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

20 June 2018

Hereditary sensorineural hearing loss associated with onychodystrophy and digital malformations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

20 June 2018

Langer-Giedion syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

20 June 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=1080027

20 June 2018

Pathogenesis of preaxial polydactyly of the hand in human embryos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

20 June 2018

A female patient with "Aase syndrome".

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

20 June 2018

Congenital hypoplastic anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

20 June 2018

Polydactyly and the triphalangeal thumb

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

20 June 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=1080027

20 June 2018

The fetal hydantoin syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

20 June 2018

Occurrence of an Additional Phalanx in the Human Pollex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

26 November 2018

Hereditary Congenital Deafness With Onychodystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

26 November 2018

Familial deafness with osteo-onycho-dysplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

26 November 2018

The Thumb in the Congenital Malformation Syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

26 November 2018

I--triphalangeal thumbs in three sibs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

26 November 2018

A syndrome of polydactyly-syndactyly and triphalangeal thumbs in three generations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1080027

26 November 2018

Congenital split foot (lobster claw) and triphalangeal thumb

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Skeletal manifestations of the Holt-Oram syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Triphalangeal thumb

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Notes on the peculiarities of the first metacarpal and the first metatarsal bones

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Triphalangeal thumb in a Bantu family

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brief clinical report: syndrome of acrofacial dysostosis, cleft lip/palate, and triphalangeal thumb in a Brazilian family

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Treatment of the triphalangeal thumb

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thalidomide embryopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Pulmonary aplasia and triphalangia of the thumb: a new association of abnormalities?]

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Triphalangeal thumb

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CONGENITAL HEART DISEASE AND UPPER-EXTREMITY DEFORMITIES: A REPORT OF TWO FAMILIES

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Five-fingered hand. One-stage pollicization of the radial finger

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Triphalangeal thumbs associated with hypoplastic anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.). I. Clinical aspects

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The lacrimo-auriculo-dento-digital syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new syndrome of triphalangeal thumbs and brachy-ectrodactyly

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Triphalangeal Thumbs

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Triphalangeal thumbs and congenital erythroid hypoplasia: Report of a case with unusual features

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Agenesis of the lung. Report of four patients with unusual anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variable expression of the Holt-Oram syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polydactyly with triphalangeal thumbs, brachydactyly, camptodactyly, congenital dislocation of the patellas, short stature and borderline intelligence

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Subcutaneous vascular abnormalities in fetal hydantoin syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Triphalangeal thumbs‐ectrodactyly in a sporadic case

1 reference

https://pubmed.ncbi.nlm.nih.gov/3050097

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.25.8.505

0 references

PMC publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

ResearchGate publication ID

0 references

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