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مکتبة رقمیه للعلوم الطبيه
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Results of search for 'au:"Hadjsalem, Ikhlass"'
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Authors
Elloumi, Moez
Fakhfakh, Faiza
Fendri-Kriaa, Nourhene
Hadjsalem, Ikhlass
Kanoun, Houda
Louhichi, Nacim
Marrakchi, Slaheddine
Masmoudi, Abderrahmen
Medhaffar, Moez
Mkaouar-Rebai, Emna
Souissi, Tawfik
Trabelsi, Fatma
Turki, Hamida
Yaïch, Firas
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Topics
Adolescent
Amino Acid Sequence
Base Sequence
Codon, Nonsense
Consanguinity
Factor XIII
Factor XIII Deficiency
Factor XIIIa
Female
Founder Effect
Frameshift Mutation
Genetic Association Studies
Genotype
Haplotypes
Humans
Male
Microsatellite Repeats
Pedigree
Tunisia
genetics
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English
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1.
Congenital lamellar ichthyosis in Tunisia is caused by a founder nonsense mutation in the TGM1 gene.
[electronic resource]
by
Louhichi, Nacim
Hadjsalem, Ikhlass
Marrakchi, Slaheddine
Trabelsi, Fatma
Masmoudi, Abderrahmen
Turki, Hamida
Fakhfakh, Faiza
Producer:
20140303
In:
Molecular biology reports
vol. 40
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Available from publisher's website
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2.
Congenital factor XIII deficiency caused by two mutations in eight Tunisian families: molecular confirmation of a founder effect.
[electronic resource]
by
Louhichi, Nacim
Medhaffar, Moez
Hadjsalem, Ikhlass
Mkaouar-Rebai, Emna
Fendri-Kriaa, Nourhene
Kanoun, Houda
Yaïch, Firas
Souissi, Tawfik
Elloumi, Moez
Fakhfakh, Faiza
Producer:
20100412
In:
Annals of hematology
vol. 89
Online resources:
Available from publisher's website
Availability:
No items available.
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