(Q34053469)

30 July 2017

title

A syndrome of congenital aplasia of the alae nasi, deafness, hypothyroidism, dwarfism, absent permanent teeth, and malabsorption (English)

1 reference

30 July 2017

0 references

1 reference

multiple abnormalities

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5171616

31 January 2024

author name string

A. Johanson

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5171616

31 January 2024

R. Blizzard

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5171616

31 January 2024

language of work or name

English

0 references

publication date

1 December 1971

1 reference

full work available at URL

30 July 2017

https://api.elsevier.com/content/article/PII:S0022347671801944?httpAccept=text/xml

1 reference

10.1016/S0022-3476(71)80194-4

DOI

https://api.crossref.org/works/10.1016/S0022-3476(71)80194-4

https://api.elsevier.com/content/article/PII:S0022347671801944?httpAccept=text/plain

31 January 2024

1 reference

10.1016/S0022-3476(71)80194-4

DOI

https://api.crossref.org/works/10.1016/S0022-3476(71)80194-4

The Journal of Pediatrics

31 January 2024

published in

1 reference

30 July 2017

volume

79

1 reference

30 July 2017

issue

6

1 reference

30 July 2017

page(s)

982-987

1 reference

Unusual case of XXY Klinefelter's syndrome with pancreatic insufficiency, hypothyroidism, deafness, chronic lung disease, dwarfism and microcephaly

30 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2871%2980194-4

Oculodentodigital dysplasia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2871%2980194-4

Absorption of Oral Thyroxine in Man

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2871%2980194-4

Familial syndrome combining deaf-mutism, stuppled epiphyses, goiter and abnormally high PBI: possible target organ refractoriness to thyroid hormone

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2871%2980194-4

Otic Lesions and Congenital Hypothyroidism in the Developing Chick*

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2871%2980194-4

10.1016/S0022-3476(71)80194-4

7 January 2021

Identifiers

DOI

1 reference

30 July 2017

1 reference