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OCA2
Oculocutaneous Albinism, a Family Matter Summer Moon, DO,* Katherine Braunlich, DO,** Howard Lipkin, DO,*** Annette Lacasse, DO***
Arielle Yablonovitch and Ye Henry Li Most People in the World Have Brown Eyes, Except in Europe
The Genetics of Human Skin and Hair Pigmentation
Human Pigmentation Variation: Evolution, Genetic Basis, and Implications for Public Health
Oculocutaneous Albinism Type 2 (OCA2) with Homozygous 2.7-Kb Deletion of the P Gene and Sickle Cell Disease in a Cameroonian Family
Genetic Causes of Oculocutaneous Albinism in Pakistani Population
Association of Five Snps with Human Hair Colour in the Polish Population
CRISPR Mutagenesis Confirms the Role of Oca2 in Melanin
Computational Investigation of the Ph Dependence of Stability of Melanosome Proteins: Implication for Melanosome Formation and Disease
P Gene As an Inherited Biomarker of Human Eye Color1
OCA2 Gene OCA2 Melanosomal Transmembrane Protein
Comparing Signals of Natural Selection Between Three Indigenous North American Populations
Interplay of Placental DNA Methylation and Maternal Insulin Sensitivity in Pregnancy
More Than Meets the Eye: the Genetics of Eye Color by Annie Prud’Homme-Généreux Life Sciences Quest University, Canada
Adaptation of Human Skin Color in Various Populations Lian Deng1,2 and Shuhua Xu1,2,3,4*
Genotype–Phenotype Associations and Human Eye Color
Document Title: Gene Polymorphism and Human Pigmentation Author: Murray H
Albinism: Epidemiology, Genetics, Cutaneous
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Interplay of Placental DNA Methylation and Maternal Insulin Sensitivity in Pregnancy Short Title
P Gene Mutations in Patients with Oculocutaneous Albinism And
Prader-Willi Syndrome
Genetic Analyses of Oculocutaneous Albinism Types 1 and 2 with Four
More Than Skin Deep: Genetics, Clinical Manifestations, and Diagnosis of Albinism
Oculocutaneous Albinism
Novel Compound Heterozygous Mutations in OCA2 Gene Associated
Gene Section Short Communication
Gender Is a Major Factor Explaining Discrepancies in Eye Colour Prediction Based on HERC2/OCA2 Genotype and the Irisplex Model
Understanding Variation in Human Skin Color Activity Educator Materials
Allele Variations in the OCA2 Gene (Pink-Eyed-Dilution Locus) Are Associated with Genetic Susceptibility to Melanoma
Accuracy of Next-Generation Sequencing for Molecular Diagnosis in Patients with Infantile Nystagmus Syndrome
Gene Interactions Contribute to Eye Colour Variation in Humans
Inheritance of a Novel Mutated Allele of the OCA2 Gene Associated with High Incidence of Oculocutaneous Albinism in a Polynesian Community