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1
Association of leptin–melanocortin gene polymorphisms with the risk of obesity in northwest Indian population
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Association of leptin–melanocortin gene polymorphisms with the risk of obesity in northwest Indian population

Sharma, Tanmayi ; Badaruddoza, Badaruddoza

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.57-18, Article 57 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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2
Consanguinity, complex diseases and congenital disabilities in the Souss population (Southern Morocco): a cross-sectional survey
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Consanguinity, complex diseases and congenital disabilities in the Souss population (Southern Morocco): a cross-sectional survey

Dahbi, Noura ; El khair, Abderrazak ; Cheffi, Khadija ; Habibeddine, Lamiaa ; Talbi, Jalal ; Hilali, Abderraouf ; El ossmani, Hicham

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.27-12, Article 27 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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3
Association of p53 codon 72 polymorphism with weight and metabolic diseases in a Central Indian population
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Association of p53 codon 72 polymorphism with weight and metabolic diseases in a Central Indian population

Abraham, Jessy ; Mahapatra, Deepak ; Agrawal, Pratishtha ; James, Mary Jovita

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.6-9, Article 6 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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4
Four microRNA gene polymorphisms are associated with Iraqi patients with colorectal cancer
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Four microRNA gene polymorphisms are associated with Iraqi patients with colorectal cancer

Jameel, Zahraa Isam

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.47-12, Article 47 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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5
BRCA mutations: screening for germ-line founder mutations among early-onset Syrian breast cancer patients
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BRCA mutations: screening for germ-line founder mutations among early-onset Syrian breast cancer patients

Wahabi Alzahabi, Salma ; Saifo, Maher ; Abou Alchamat, Ghalia

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.18-7, Article 18 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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6
ACE I/D polymorphism in cognitive impairment and depression among North Indian adults: a pilot study
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ACE I/D polymorphism in cognitive impairment and depression among North Indian adults: a pilot study

Sharma, Apoorva ; Chaudhary, Vineet ; Thakur, Mamta Kumari ; Devi, Naorem Kiranmala ; Saraswathy, Kallur Nava

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.43-7, Article 43 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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7
Genomic susceptibility to gastric cancer in Northwest Iran: population-based and case–control studies
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Genomic susceptibility to gastric cancer in Northwest Iran: population-based and case–control studies

Aghghaleh, Homa Akhavan ; Ranji, Najmeh ; Habibollahi, Hadi

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.41-15, Article 41 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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8
Association of VEGF-2549I/D promoter polymorphism with gastrointestinal tract cancer risk: a meta-analysis
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Association of VEGF-2549I/D promoter polymorphism with gastrointestinal tract cancer risk: a meta-analysis

Mahajan, Deepanshi ; Sambyal, Vasudha ; Guleria, Kamlesh

Egyptian Journal of Medical Human Genetics, 2024-06, Vol.25 (1), p.65-12, Article 65 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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9
Association of single nucleotide polymorphism at BMP2 gene with iron deficiency status among anaemic patients in Hospital Universiti Sains Malaysia
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Association of single nucleotide polymorphism at BMP2 gene with iron deficiency status among anaemic patients in Hospital Universiti Sains Malaysia

Azman, Nur Ain ; Zulkafli, Zefarina ; Bakar, Nur Salwani ; Assyuhada, Mat Ghani Siti Nor ; Mohammad, Siti Nur Nabeela A’ifah

Egyptian Journal of Medical Human Genetics, 2024-04, Vol.25 (1), p.46-8, Article 46 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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10
cxsAssociation study between single nucleotide polymorphism in thrombospondins THBS1 gene and THBS2 gene and coronary artery disease in Indian population
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cxsAssociation study between single nucleotide polymorphism in thrombospondins THBS1 gene and THBS2 gene and coronary artery disease in Indian population

Eba, Ale ; Raza, Syed Tasleem ; Wani, Irshad A. ; Siddiqi, Zeba ; Abbas, Mohammad ; Srivastava, Sanchita ; Mahdi, Farzana

Egyptian Journal of Medical Human Genetics, 2024-02, Vol.25 (1), p.26-8, Article 26 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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