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Research article

First published 1999-09

Mutations in Exon 3 of the PAH Gene Causing Mild Hyperphenylalaninemia

Cezary Zekanowski, Maria Nowacka, Maria Gizewska [...]

Genetic Testing and Molecular Biomarkers

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Abstract

First published 2020-4

Mutational Analysis Revealed Polymorphic Variants in Exon 3 and Exon 4 Of P53 Gene in Cervical Cancer

Omotoso Olabode, A. Gbadegesin Michael, A. O. Oluwasola Timothy [...]

Tumori Journal

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Research article

First published 2012-5

Analysis of β-Catenin Expression and Exon 3 Mutations in Pediatric Sporadic Aggressive Fibromatosis

Ning Bo, Dahui Wang, Bingbing Wu [...]

Pediatric and Developmental Pathology

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Research article

First published 2013-4

Autosomal-dominant Meesmann epithelial corneal dystrophy without an exon mutation in the keratin-3 or keratin-12 gene in a Chinese family

Wei Cao, Ming Yan, QianYun Hao [...]

Journal of International Medical Research

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Research article

First published 2013-3

Alteration in E-Cadherin/β-Catenin Expression in Canine Melanotic Tumors

J.-I. Han, Y. Kim, D.-Y. Kim [...]

Veterinary Pathology

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Research article

First published 2012-03

Consecutive Mutational Events in a TSHR Allele of Arab Families with Resistance to Thyroid Stimulating Hormone

Chutintorn Sriphrapradang, Alina German, Alexandra M. Dumitrescu [...]

Thyroid®

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Research article

First published 2006-2

Genetic Variants of the NOTCH3 Gene in Migraine—A Mutation Analysis and Association Study

S Schwaag, S Evers, A Schirmacher [...]

Cephalalgia

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Research article

First published 2016-2

The association of endoplasmic reticulum aminopeptidase-1 (ERAP-1) with Familial Mediterranean Fever (FMF)

Gülbüz Sezgin, Reşat Dabak, Fatih Oner Kaya [...]

United European Gastroenterology Journal

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Research article

First published 1998-11

The Extracellular Thyrotropin Receptor Domain Is Not a Major Candidate for Mutations in Toxic Thyroid Nodules

Dagmar Führer, Constanze Kubisch, Ursula Scheibler [...]

Thyroid®

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Research article

First published 2003-12

Thyroperoxidase Gene Mutations in Congenital Goitrous Hypothyroidism with Total and Partial Iodide Organification Defect

Antonio C. Nascimento, Dulce R. Guedes, Cecilia S. Santos [...]

Thyroid®

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