(Q38534241)

3 September 2017

title

Dental abnormalities as a component of the Laurence-Moon-Bardet-Biedl syndrome (English)

1 reference

3 September 2017

Kobrin JL

1

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3 September 2017

Ternand CL

series ordinal

2

1 reference

3 September 2017

Knobloch WH

series ordinal

3

1 reference

3 September 2017

Johnson DD

series ordinal

4

1 reference

3 September 2017

publication date

1 December 1990

1 reference

Ophthalmic Paediatrics and Genetics

3 September 2017

published in

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3 September 2017

volume

11

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3 September 2017

issue

4

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3 September 2017

page(s)

299-303

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Retinal and neurologic findings in the Laurence-Moon-Bardet-Biedl phenotype

3 September 2017

cites work

1 reference

https://api.crossref.org/works/10.3109%2F13816819009015717

HYPOGONADOTROPHIC HYPOGONADISM IN THE LAURENCE-MOON SYNDROME.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819009015717

Evaluation of the hypothalamic-pituitary-gonadal function in the Bardet-Biedl syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819009015717

The syndrome of Laurence-Moon-Bardet-Biedl and allied diseases in Switzerland. Clinical, genetic and epidemiological studies

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819009015717

The Laurence-Moon syndrome with germinal aplasia of the testis: report of a case and review

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819009015717

A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819009015717

Seven hereditary syndromes with pigmentary retinopathy. A review and differential diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819009015717

10.3109/13816819009015717

21 January 2018

Identifiers

DOI

1 reference

3 September 2017

1 reference