(Q35569157)

8 August 2017

title

The tricho-dento-osseous (TDO) syndrome (English)

1 reference

8 August 2017

Lichtenstein J

1

1 reference

8 August 2017

Warson R

2

1 reference

8 August 2017

Jorgenson R

3

1 reference

8 August 2017

Dorst JP

4

1 reference

8 August 2017

McKusick VA

5

1 reference

8 August 2017

language of work or name

English

0 references

publication date

1 September 1972

1 reference

American Journal of Human Genetics

8 August 2017

published in

1 reference

8 August 2017

volume

24

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8 August 2017

issue

5

1 reference

8 August 2017

page(s)

569-582

1 reference

A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration

8 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762186

Fluoride treatment of bone rarefaction in multiple myeloma and osteoporosis. A review.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762186

Osteopetrosis. A clinical, genetic, metabolic, and morphologic study of the dominantly inherited, benign form

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762186

On the possible clinical significance of thyrocalcitonin and of osteosclerosis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762186

Parathyroid hormone action: definition of problems

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762186

Developmental affections of the skeleton characterized by osteosclerosis.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762186

Hereditary enamel hypoplasia: its association with characteristic hair structure

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762186

Congenital stenosis of medullary spaces in tubular bones and calvaria in two proportionate dwarfs--mother and son; coupled with transitory hypocalcemic tetany

24 October 2018

1 reference

12 December 2020

Idiopathic osteosclerosis. A report of 6 related cases

1 reference

12 December 2020

Sclerotic bone lesions

1 reference

12 December 2020

Hereditary amelogenesis imperfecta. A rare autosomal dominant type

1 reference

12 December 2020

Hyperostosis corticalis generalisata. Report of seven cases

1 reference

12 December 2020

DOMINANT HEREDITARY SYNDROME, COMBINING CRANIO-FACIAL DYSOSTOSIS PECULIAR TYPE, GROWTH INSUFFICIENCY OF CHONDRODYSTROPHIC APPEARANCE, AND MASSIVE THICKENING OF OF THE CORTICES OF LONG BONES

1 reference

12 December 2020

Identifiers

PMC publication ID

1762186

1 reference

8 August 2017

1 reference