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- 270 Genes Genetic Insights Panel
- The Eye in the Hermansky-Pudlak Syndrome: a Literature Review
- WES Gene Package Hearing Impairment.Xlsx
- Genomeposter2009.Pdf
- Hermansky-Pudlak Syndrome and Oculocutaneous Albinism in Chinese Children with Pigmentation Defects and Easy Bruising Bradley Power1, Carlos R
- Waardenburg Syndrome and Homoeopathy
- Excluded Conditions
- Blueprint Genetics Hermansky-Pudlak Syndrome Panel
- Prospective Study of the Phenotypic and Mutational Spectrum of Ocular Albinism and Oculocutaneous Albinism
- Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders
- Genetics of the Evolutionary Process
- Jules Stein Eye Institute Itute
- Hearing and Vision Loss Next- Generation Sequencing Panel
- Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the Babyseq Project
- Albinism: Epidemiology, Genetics, Cutaneous
- Egyptian Journal of Medical Human Genetics (2010) 11, 167–172
- ORPHA Number Disease Or Group of Diseases 300305 11P15.4
- Genetic Disorders of Pigmentation
- Albinism What Is Albinism? When Someone Has Albinism, Their Body Has Trouble Creating Pigment
- The Genetics of Deafness
- Biology and Genetics of Oculocutaneous Albinism and Vitiligo – Common Pigmentation Disorders in Southern Africa
- More Than Skin Deep: Genetics, Clinical Manifestations, and Diagnosis of Albinism
- Primary Adrenal Insufficiency in Children
- Nystagmus and Related Ocular Motility Disorders
- Waardenburg Syndrome
- Ocular Albinism
- Matthew Roe, OD; Alexandria Tilley, OD; Andrea Thau, OD, FCOVD, FAAO, DPNAP
- Three Cases of Waardenburg Syndrome Type 2 in a Korean Family
- WES Gene Package Multiple Congenital Anomalie
- The Morbid Anatomy of the Human Genome: Chromosomal Location of Mutations Causing Disease
- Type 1 Established Condition List
- Purpose and Hypothesis
- Clinical Medical Policy
- Whole Exome Sequencing Gene Package Hearing Impairment, Version 6.1, 31-1-2020
- Prevalence and Incidence of Rare Diseases: Bibliographic Data
- Albinism in Life
- Prevalence and Incidence of Rare Diseases
- Ocular Albinism Br J Ophthalmol: First Published As 10.1136/Bjo.77.4.222 on 1 April 1993
- Blueprint Genetics Albinism Panel
- Oculocutaneous Albinism Precision Panel Overview
- A Case of Behcet's Disease in a Patient with Albinism
- Newborn Genetic Analysis
- Clinical and Morphological Features of Waardenburg Syndrome Type II
- Children's Special Health Services
- To View Fulltext
- Clinical and Genetic Variability in Children with Partial Albinism Patrick Campbell1,6, Jamie M