(Q28253439)

English

A familial syndrome of short stature associated with facial dysplasia and genital anomalies

scientific article published on November 1, 1970

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A familial syndrome of short stature associated with facial dysplasia and genital anomalies (English)

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author name string

D. Aarskog

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1

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Europe PubMed Central

PubMed ID

5504078

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5504078

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English

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publication date

November 1970

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full work available at URL

https://api.elsevier.com/content/article/PII:S0022347670802475?httpAccept=text/xml

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DOI

10.1016/S0022-3476(70)80247-5

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https://api.crossref.org/works/10.1016/S0022-3476(70)80247-5

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26 May 2023

https://api.elsevier.com/content/article/PII:S0022347670802475?httpAccept=text/plain

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Crossref

DOI

10.1016/S0022-3476(70)80247-5

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https://api.crossref.org/works/10.1016/S0022-3476(70)80247-5

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26 May 2023

published in

The Journal of Pediatrics

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volume

77

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page(s)

856-61

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issue

5

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cites work

Compendium on shortness of stature

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7 January 2021

THE TURNER PHENOTYPE IN THE MALE

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7 January 2021

Hypertelorism With Turner Phenotype

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7 January 2021

Growth-hormone deficiency in man: an isolated, recessively inherited defect

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7 January 2021

Hereditary pituitary dwarfism with spontaneous puberty

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7 January 2021

Turner's phenotype in the male

series ordinal

5

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DOI

10.1016/S0022-3476(70)80247-5

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https://api.crossref.org/works/10.1016/S0022-3476(70)80247-5

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26 May 2023

Direct Familial Transmission of the Turner Phenotype

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6

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10.1016/S0022-3476(70)80247-5

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https://api.crossref.org/works/10.1016/S0022-3476(70)80247-5

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26 May 2023

Familial occurrence of the somatic phenotype of Turner's syndrome

series ordinal

8

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DOI

10.1016/S0022-3476(70)80247-5

reference URL

https://api.crossref.org/works/10.1016/S0022-3476(70)80247-5

retrieved

26 May 2023

Identifiers

DOI

10.1016/S0022-3476(70)80247-5

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PubMed ID

5504078

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(Q28253439)

A familial syndrome of short stature associated with facial dysplasia and genital anomalies

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