3M syndrome: A Tunisian seven-cases series

Author:

Khachnaoui-Zaafrane Khaoula,Ouertani InesORCID,Zanati Amira,Kandara Hajer,Maazoul Faouzi,Mrad Ridha

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference34 articles.

1. Consanguinity and endogamy in Northern Tunisia and its impact on non-syndromic deafness;Arab;Genet. Epidemiol.,2004

2. Hip dislocation in 3-M syndrome;Badina;Clin. Dysmorphol.,2011

3. An organelle-specific protein landscape identifies novel diseases and molecular mechanisms;Boldt;Nat. Commun.,2016

4. 3-M slender-boned nanism. An intrauterine growth retardation syndrome;Cantú;Am. J. Dis. Child.,1981

5. Exploring the spectrum of 3-M syndrome, a primordial short stature disorder of disrupted ubiquitination;Clayton;Clin. Endocrinol.,2012

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