The tricho-dento-osseous (TDO) syndrome (Q35569157)

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scientific article published on September 1972

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Language	Label	Description	Also known as
English	The tricho-dento-osseous (TDO) syndrome	scientific article published on September 1972

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5054226

retrieved

8 August 2017

title

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

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5054226

retrieved

8 August 2017

author name string

Lichtenstein J

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5054226

retrieved

8 August 2017

Warson R

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5054226

retrieved

8 August 2017

Jorgenson R

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5054226

retrieved

8 August 2017

Dorst JP

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5054226

retrieved

8 August 2017

McKusick VA

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5054226

retrieved

8 August 2017

language of work or name

English

0 references

publication date

1 September 1972

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5054226

retrieved

8 August 2017

published in

American Journal of Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5054226

retrieved

8 August 2017

volume

24

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5054226

retrieved

8 August 2017

issue

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5054226

retrieved

8 August 2017

page(s)

569-582

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stated in

Europe PubMed Central

PubMed publication ID

5054226

retrieved

8 August 2017

cites work

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

27 July 2018

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

27 July 2018

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

27 July 2018

On the possible clinical significance of thyrocalcitonin and of osteosclerosis

1 reference

stated in

PubMed Central

reference URL

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

retrieved

27 July 2018

Parathyroid hormone action: definition of problems

1 reference

stated in

PubMed Central

reference URL

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

retrieved

27 July 2018

Developmental affections of the skeleton characterized by osteosclerosis.

1 reference

stated in

PubMed Central

reference URL

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

retrieved

26 September 2018

Hereditary enamel hypoplasia: its association with characteristic hair structure

1 reference

stated in

PubMed Central

reference URL

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

retrieved

24 October 2018

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5054226

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Idiopathic osteosclerosis. A report of 6 related cases

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5054226

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sclerotic bone lesions

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5054226

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary amelogenesis imperfecta. A rare autosomal dominant type

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5054226

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperostosis corticalis generalisata. Report of seven cases

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5054226

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5054226

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1762186

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5054226

retrieved

8 August 2017

PubMed publication ID

5054226

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5054226

retrieved

8 August 2017

 

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