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Microphthalmia
National Study of Microphthalmia, Anophthalmia, and Coloboma (MAC
A Case of Hallermann-Streiff Syndrome with Aphakia
Novel Mutations in ALDH1A3 Associated with Autosomal Recessive Anophthalmia/ Microphthalmia, and Review of the Literature Siying Lin1, Gaurav V
A Novel Keratocan Mutation Causing Autosomal Recessive Cornea Plana
Molecular Genetics of Corneal Dystrophy
A New Phenotype of Recessively Inherited Foveal Hypoplasia and Anterior Segment Dysgenesis Maps to a Locus on Chromosome 16Q23.2–24.2
The Rieger Syndrome: a Case Report with Unusual Dental Findings
Whole Exome Sequencing in Coloboma/Microphthalmia: Identification of Novel and Recurrent Variants in Seven Genes
Surgical Correction of Hallermann-Streiff Syndrome: a Case Report of Esotropia, Entropion, and Blepharoptosis
Clinical and Molecular Characterization of a Family with Autosomal Recessive Cornea Plana
Aniridia (PAX6) Sequencing & Deletion/Duplication
Ocular Abnormalities in the Myopathic Hamster (UM-X7.1 Strain)
Ocular Manifestations of Inherited Diseases Maya Eibschitz-Tsimhoni
Congenital Aniridia Congenital Aniridia
Breed Predisposition to Eye Disease in the Ten Most Common Purebred Dogs in Ireland
Congenital Microphthalmia with Intraorbital Cyst: a Rare Case Report
Another Observation of Microphthalmia in an XX Male: Microphthalmia with Linear Skin Defects Syndrome Without Linear Skin Lesions
Early Vitrectomy Effective for Norrie Disease
Top View
Premature Ovarian Insufficiency As a Variable Feature Of
Ecvo Manual: Breeds 2021
Novel Mutation in CRYBB3 Causing Pediatric Cataract and Microphthalmia
Microphthalmia
HSVMA Guide to Congenital and Heritable Disorders in Dogs
Lenz Microphthalmia Syndrome
Diagnosis of Complicated FEVR Preoperatively and Intra-/Post
Familial Exudative Vitreoretinopathy
The Molecular Basis of Human Anophthalmia and Microphthalmia
Inherited PAX6, NF1 and OTX2 Mutations in a Child with Microphthalmia and Aniridia
Congenital Corneal Opacities KK Nischal 1327
ALDH1A3 Loss of Function Causes Bilateral Anophthalmia/Microphthalmia and Hypoplasia of the Optic Nerve and Optic Chiasm
Open Access: Ejournal.Unud.Ac.Id
Leading Simulators of Retinoblastoma
A Case with Microphthalmia and Multiple Congenital Anomalies Mikroftalmi Ve Çoklu Konjenital Anomalili Bir Olgu
The Ohdo Blepharophimosis Syndrome: a Third Case
CRYAA Nucleotide Variants to a Complex Presentation of Anterior Segment Dysgenesis Andrey V
Streiff&Ndash;Francois Syndrome: Report of Four Cases
Microcornea-Cataract Syndrome
Ophthalmological Features Associated with COL4A1 Mutations
A Genetic Linkage Study of a Family with Norrie's Disease
Phenotypic Overlap Between Familial Exudative Vitreoretinopathy and Microcephaly, Lymphedema, and Chorioretinal Dysplasia Caused by KIF11 Mutations
Grand Rounds
Deletion of G Protein-Coupled Receptor 48 Leads to Ocular Anterior Segment Dysgenesis (ASD) Through Down-Regulation of Pitx2
The Genetic Associations of Rhegmatogenous Retinal
Genetics Underlying the Interactions Between Neural Crest Cells and Eye Development
Bilateral Microphthalmia and Aphakia Associated with Multiple Eye Abnormalities in a Free-Living European Red Deer Calf (Cervus Elaphus)
How Ectodermal Dysplasias Affects Eyes and How to Treat
Identification of Novel KIF11 Mutations in Patients with Familial Exudative
Linear Skin Defects with Multiple Congenital Anomalies (LSDMCA): an Unconventional Mitochondrial Disorder
A Case with Microphthalmia and Multiple Congenital Anomalies Mikroftalmi Ve Çoklu Konjenital Anomalili Bir Olgu
Animaleyediseases 5X7 Booklet
Unique Contact Lens Fitting Challenges in Microphthalmia
Genotype Phenotype Correlation and Variability in Microcephaly Associated with Chorioretinopathy Or Familial Exudative Vitreoretinopathy
Coloboma Coloboma Describes Conditions Where Normal Tissue in Or Around the Eye Is Missing from Birth
Blueprint Genetics Microphthalmia, Anophthalmia and Anterior
An Update on the Genetics of Ocular Coloboma
Corneal Dystrophies Precision Panel Overview Indications Clinical Utility
Recurrent Heterozygous PAX6 Missense Variants Cause Severe Bilateral Microphthalmia Via Predictable Effects on Dnaâ
Blueprint Genetics Ectopia Lentis Panel
A Practical Guide to the Management of Anophthalmia and Microphthalmia
Probably Norrie's Disease Due to Mutation
Eoftalmo Eyeball Malformations – Microphthalmia, Anophthalmia, and Coloboma
Congenital Microphthalmia with Orbital Cyst: a Case Series
Genetics of Anophthalmia and Microphthalmia. Part 2: Syndromes Associated with Anophthalmia–Microphthalmia