(Q33596953)

28 July 2017

title

An epidemiological and genetic study of congenital profound deafness in Tunisia (governorate of Nabeul) (English)

1 reference

28 July 2017

0 references

1 reference

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Ben Arab S

1

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28 July 2017

Bonaïti-Pellié C

series ordinal

2

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28 July 2017

Belkahia A

series ordinal

3

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28 July 2017

language of work or name

English

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publication date

1 January 1990

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

27

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28 July 2017

issue

1

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28 July 2017

page(s)

29-33

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ESTIMATION OF PREVALENCE UNDER INCOMPLETE SELECTION.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016876

Genetic tests under incomplete ascertainment

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016876

A unified model for complex segregation analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016876

Studies on an isolated West Indies population: IV. Genetic study of hearing loss

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016876

Studies on an isolated West Indies population. III. Epidemiologic study of sensorineural hearing loss

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016876

Segregation analysis in human genetics

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2308153

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.27.1.29

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28 July 2017

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28 July 2017

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