Camptomelic dwarfism. A genetically determined mesenchymal disorder combined with sex reversal (Q67013316)

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2 September 2019

title

Camptomelic dwarfism. A genetically determined mesenchymal disorder combined with sex reversal (English)

1 reference

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2 September 2019

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

13 July 2023

author name string

M. L. Hovmöller

1

1 reference

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11 July 2022

A. Osuna

2

1 reference

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11 July 2022

O. Eklöf

3

1 reference

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11 July 2022

K. Fredga

4

1 reference

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11 July 2022

A. Hjerpe

5

1 reference

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11 July 2022

J. Linsten

6

1 reference

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11 July 2022

M. Ritzen

7

1 reference

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11 July 2022

V. Stanescu

8

1 reference

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11 July 2022

N. Svenningsen

9

1 reference

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11 July 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=561769

11 July 2022

publication date

1 January 1977

1 reference

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2 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:561769%20AND%20SRC:MED&resulttype=core&format=json

2 September 2019

volume

86

1 reference

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2 September 2019

issue

1

1 reference

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2 September 2019

page(s)

51-62

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:561769%20AND%20SRC:MED&resulttype=core&format=json

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

2 September 2019

cites work

1

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

Congenital bowing of the long bones: report of a case

13 July 2023

5

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

13 July 2023

Camptomelic dwarfism

6

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

The inheritance of the aarskog facial-digital-genital syndrome

13 July 2023

7

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

Familial occurrence of persistent Mullerian structures in otherwise normal males.

13 July 2023

8

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

Autosomal recessive inheritance in camptomelic dwarfism.

13 July 2023

10

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

The aetiology and management of intersexuality

13 July 2023

11

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

X-Y chromosomal interchange in the aetiology of true hermaphroditism and of XX Klinefelter's syndrome

13 July 2023

12

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

Genetics and immunology of sex-linked antigens

13 July 2023

14

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

46, XY female: anti-androgenic effect of oral contraceptive?

13 July 2023

15

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

Growth of interorbital distance and skull thickness as observed in roentgenographic measurements.

13 July 2023

17

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

13 July 2023

Camptomelic dwarfism

19

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

In Vitro Synthesis of Mullerian-Inhibiting Hormone by Seminiferous Tubules Isolated from the Calf Fetal Testis

13 July 2023

20

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

The "campomelic" syndrome. Short life-span dwarfism with respiratory distress, hypotonia, peculiar facies, and multiple skeletal and cartilaginous deformities

13 July 2023

24

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

13 July 2023

A variant of campomelia

31

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

The campomelique syndrome

13 July 2023

33

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

The campomelic syndrome. Congenital bowing of limbs and other skeletal and extraskeletal anomalies

13 July 2023

36

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

Congenital bowing of the long bones in two sisters

13 July 2023

37

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

Familial camptomelic dwarfism

13 July 2023

38

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

Possible role for H--Y antigen in the primary determination of sex

13 July 2023

39

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

Serologic detection of a y-linked gene in xx males and xx true hermaphrodites

13 July 2023

40

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

Familial incomplete male pseudohermaphroditism, type 2. Decreased dihydrotestosterone formation in pseudovaginal perineoscrotal hypospadias.

13 July 2023

41

1 reference

https://api.crossref.org/works/10.1111/J.1601-5223.1977.TB01212.X

13 July 2023

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:561769%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

2 September 2019

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1111/j.1601-5223.1977.tb01212.x

1 reference