Comorbidity in the Tunisian population.

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Genetics and genomic medicine in Tunisia.Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome

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Comorbidity in the Tunisian population.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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2015年论文

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2015年论文

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name

Comorbidity in the Tunisian population.

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Comorbidity in the Tunisian population.

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type

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label

Comorbidity in the Tunisian population.

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Comorbidity in the Tunisian population.

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prefLabel

Comorbidity in the Tunisian population.

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Comorbidity in the Tunisian population.

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P1476

Comorbidity in the Tunisian population.

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C Charfeddine

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C Naouali

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G O Tadmouri

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G Romeo

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I Chabchoub

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K Monastiri

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L Cherif Ben Abdallah

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L Romdhane

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M Hachicha

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P2860

Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness

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Homozygosity mapping and whole-exome sequencing to detect SLC45A2 and G6PC3 mutations in a single patient with oculocutaneous albinism and neutropenia

Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family.

Genetic homogeneity of mutational spectrum of group-A xeroderma pigmentosum in Tunisian patients.

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312-319

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scholarly article

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10.1111/CGE.12616

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Sonia Abdelhak

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2015-05-22T00:00:00Z

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Comorbidity in the Tunisian population.

about

P2860

P2860

Comorbidity in the Tunisian population.

description

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type

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P1476

P2093

P2860

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P698