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Image of Identification of Mutation in Exon2 of the NKX2.5 Gene in Bangladeshi Pediatric Patients with Congenital Hypothyroidism

Thesis

Identification of Mutation in Exon2 of the NKX2.5 Gene in Bangladeshi Pediatric Patients with Congenital Hypothyroidism

Dr. Marjia Khatun - Personal Name;

Course: MS, Guide: Prof. Dr. Laila Anjuman Banu

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T-5119

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Detail Information

Call Number: -
Publisher: BSMMU : Dr. Marjia Khatun., 2020
Collation: i-xxv, 1-81, ii-lxv
Language: English
Subject(s): Anatomy

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Identification of Mutation in Exon2 of the NKX2.5 Gene in Bangladeshi Pediatric Patients with Congenital Hypothyroidism

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