(Q33596753)

28 July 2017

Hereditary multiple exostoses. (English)

1 reference

hereditary multiple exostoses

28 July 2017

1 reference

Hennekam RC

1

1 reference

PubMed ID

1856833

28 July 2017

language of work or name

English

0 references

publication date

1 April 1991

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

28

1 reference

28 July 2017

262-266

1 reference

28 July 2017

4

1 reference

Studies on the Anatomical Changes which accompany certain Growth-disorders of the Human Body: I. The Nature of the Structural Alterations in the Disorder known as Multiple Exostoses

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Dysplasia epiphysealis hemimelica. A report of fifteen cases and a review of the literature

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

HEREDITARY MULTIPLE EXOSTOSIS

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Upper limb involvement in the Klein-Waardenburg 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=1016830

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Hereditary multiple exostoses with spinal cord compression

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

The tricho-rhino-phalangeal syndrome with exostoses (or Langer-Giedion syndrome): four additional patients without mental retardation and review of the literature

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Namaqualand hip dysplasia: an autosomal dominant entity.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

The infrequency of malignant disease in diaphyseal aclasis and neurofibromatosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Upington disease: a familial dyschondroplasia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Multiple exostoses of bone with fatal spinal cord compression: Report of a case and brief review of the literature

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Humero-Spinal Dysostosis With Congenital Heart Disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Osteochondromas as a cause of false popliteal aneurysms. Review of the literature and report of two cases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Periodic hypersomnia, congenital ectodermal disorders and multiple exostosis.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Multiple hereditary osteochondromata

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Shoulder girdle dysplasia associated with nail patella syndrome. A case report and literature review

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Maternal origin of a de novo chromosome 8 deletion in a patient with Langer-Giedion 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=1016830

Genomic imprinting: review and relevance to human diseases.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Hereditary Multiple Exostosis: A comparative genetic evaluation in man and horses

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Cerebro-Facio-Thoracic Dysplasia: Report of Three Cases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Multiple cartilaginous exostoses with polyposis of stomach and colon: a new, hereditary combination different from Gardner's syndrome (author's transl)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Hereditary multiple exostoses: clinicopathologic features of a comparative study in horses and man

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Hereditary multiple exostoses. Anthropometric, roentgenographic, and clinical 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=1016830

Multiple cartilaginous exostoses and neoplastic degeneration: review of the literature (author's transl)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Frontometaphyseal dysplasia--evidence for X-linked inheritance.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Familial multiple exostoses—no chromosome 8 deletion observed

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016830

Spontaneous resolution of an osteochondroma

30 October 2018

1 reference

12 December 2020

Influence of denervated muscles on exostoses of rats fed a sweet-pea diet

1 reference

12 December 2020

DNA polymorphism analysis of hereditary multiple exostoses in horses

1 reference

12 December 2020

New syndrome: Exostoses, anetodermia, brachydactyly

1 reference

12 December 2020

The tricho-rhino-phalangeal syndrome(s): chromosome 8 long arm deletion: is there a shortest region of overlap between reported cases? TRP I and TRP II syndromes: are they separate entities?

1 reference

12 December 2020

Hereditary multiple exostosis. A comparative human-equine-epidemiologic study

1 reference

12 December 2020

The treatment of hereditary multiple exostosis of the upper extremity

1 reference

12 December 2020

Osteomesopyknosis. Case report

1 reference

12 December 2020

Severe mental retardation in a patient with tricho-rhino-phalangeal syndrome type I and 8q deletion

1 reference

12 December 2020

Exostosis: development, evolution and relationship to malignant degeneration

1 reference

12 December 2020

Osteomesopyknosis: An autosomal dominant osteosclerosis

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.28.4.262

1 reference

28 July 2017

1 reference

28 July 2017

1 reference

PubMed ID

1856833