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Items: 1 to 20 of 129

1.

Genetic diseases in the Tunisian population.

Romdhane L, Abdelhak S; Research Unit on Molecular Investigation of Genetic Orphan Diseases; Collaborators.

Am J Med Genet A. 2011 Jan;155A(1):238-67. doi: 10.1002/ajmg.a.33771. Review.

PMID:
21204241
2.

Specific aspects of consanguinity: some examples from the Tunisian population.

Romdhane L, Ben Halim N, Rejeb I, Kefi R, Bouyacoub Y, Ben Rekaya M, Messai H, Messaoud O, Riahi Z, Bonnet C, Ben Rhouma F, Nagara M, Petit C, McElreavey K, Romeo G, Abdelhak S.

Hum Hered. 2014;77(1-4):167-74. doi: 10.1159/000362167. Epub 2014 Jul 29. Review.

PMID:
25060280
3.

Hurler disease (mucopolysaccharidosis type IH): clinical features and consanguinity in Tunisian population.

Chkioua L, Khedhiri S, Ben Turkia H, Chahed H, Ferchichi S, Ben Dridi MF, Laradi S, Miled A.

Diagn Pathol. 2011 Nov 10;6:113. doi: 10.1186/1746-1596-6-113.

4.

Founder mutations in Tunisia: implications for diagnosis in North Africa and Middle East.

Romdhane L, Kefi R, Azaiez H, Ben Halim N, Dellagi K, Abdelhak S.

Orphanet J Rare Dis. 2012 Aug 21;7:52. doi: 10.1186/1750-1172-7-52.

5.

Molecular basis of autosomal recessive diseases among the Palestinian Arabs.

Zlotogora J.

Am J Med Genet. 2002 May 1;109(3):176-82.

PMID:
11977175
6.

Autosomal recessive diseases among Palestinian Arabs.

Zlotogora J.

J Med Genet. 1997 Sep;34(9):765-6.

7.

Autosomal recessive disorders in Saguenay-Lac-Saint-Jean (Quebec, Canada): a study of inbreeding.

De Braekeleer M, Gauthier S.

Ann Hum Genet. 1996 Jan;60(Pt 1):51-6.

PMID:
8835098
8.

Genetic disorders among Palestinian Arabs: 1. Effects of consanguinity.

Zlotogora J.

Am J Med Genet. 1997 Feb 11;68(4):472-5.

PMID:
9021024
9.

Genetic diversity among the Arabs.

Teebi AS, Teebi SA.

Community Genet. 2005;8(1):21-6. Review.

PMID:
15767750
10.

Map of autosomal recessive genetic disorders in Saudi Arabia: concepts and future directions.

Al-Owain M, Al-Zaidan H, Al-Hassnan Z.

Am J Med Genet A. 2012 Oct;158A(10):2629-40. doi: 10.1002/ajmg.a.35551. Epub 2012 Aug 17.

PMID:
22903695
11.
12.

[Hereditary ichthyosis in Tunisia: epidemiological study of 60 cases].

Kharfi M, El Fekih N, Ammar D, Khaled A, Fazaa B, Ridha Kamoun M.

Tunis Med. 2008 Nov;86(11):983-6. French.

PMID:
19213489
13.

Mutations of a country: a mutation review of single gene disorders in the United Arab Emirates (UAE).

Al-Gazali L, Ali BR.

Hum Mutat. 2010 May;31(5):505-20. doi: 10.1002/humu.21232. Review.

PMID:
20437613
14.

Consanguinity and endogamy in Northern Tunisia and its impact on non-syndromic deafness.

Ben Arab S, Masmoudi S, Beltaief N, Hachicha S, Ayadi H.

Genet Epidemiol. 2004 Jul;27(1):74-9.

PMID:
15185405
15.

Genetic disorders among Palestinian Arabs: 3. Autosomal recessive disorders in a single village.

Zlotogora J, Shalev S, Habiballah H, Barjes S.

Am J Med Genet. 2000 Jun 19;92(5):343-5.

PMID:
10861664
16.

[Epidemiology of hereditary diseases in Russian population].

Ginter EK.

Vestn Ross Akad Med Nauk. 1999;(11):7-11. Review. Russian.

PMID:
10635745
17.

A novel missense mutation in the Connexin 26 gene associated with autosomal recessive nonsyndromic sensorineural hearing loss in a consanguineous Tunisian family.

Alemanno MS, Cama E, Santarelli R, Carella M, Zelante L, Toffolatti L, Palladino T, Melchionda S, Arslan E.

Int J Pediatr Otorhinolaryngol. 2009 Jan;73(1):127-31. doi: 10.1016/j.ijporl.2008.09.019. Epub 2008 Nov 5.

PMID:
18990456
18.

Consanguinity and genetic disorders. Profile from Jordan.

Hamamy HA, Masri AT, Al-Hadidy AM, Ajlouni KM.

Saudi Med J. 2007 Jul;28(7):1015-7.

PMID:
17603701
19.

[Medico-genetic study of the population of Uzbekistan. VII. Variability of hereditary pathology in 4 regions of Khorezm province].

Ginter EK, Budagova KA, Revazov AA, Krasnopol'skaia KD, Dadali EL.

Genetika. 1986 Feb;22(2):312-21. Russian.

PMID:
2937687
20.

[Medical-genetic study of the population of Lenkoran district of Azerbaijan Republic].

Dashdamirova GS, Alieva KA.

Tsitol Genet. 2009 Jul-Aug;43(4):49-55. Russian.

PMID:
19938647
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