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Fraser syndrome
Understanding Fraser Syndrome
Cryptophthalmos Syndrome: a Case Report
Fraser Syndrome: Case Report in Lacrimal System Síndrome De Fraser: Relato De Caso Nas Vias Lacrimais
Genetics of Congenital Hand Anomalies
Orphanet Report Series Rare Diseases Collection
Fraser Syndrome: Epidemiological Study in a European Population
Soonerstart Automatic Qualifying Syndromes and Conditions
Essential Genetics 5
Malformation Syndromes: a Review of Mouse/Human Homology
A Case of Fraser Syndrome Melekoglu R, Azimov R, Celik E Inonu University School of Medicine Department of Obstetrics and Gynecology, Malatya, Turkey
Fraser Syndrome
Omphalocele and Gastroschisis Precision Panel Overview Indications Clinical Utility
EUROCAT Syndrome Guide
Clinical Review Laryngotracheal Anomalies in Children with Craniofacial Syndromes
Genetic Basis of Human Congenital Anomalies of the Kidney and Urinary Tract
Prenatal Microarray Disorders List V19.1
Fraser Syndrome Adnan Aslam Saleem and Sorath Noorani Siddiqui
Ambiguous Genitalia in Neonates: a 4-Year Prospective Study in a Localized Area A.N
Top View
Lacrimal Surgery in Patients with Congenital Cranial Or Facial Anomalies
Excluded Conditions
Fraser Syndrome: Phenotypic Variability and Unusual findings in Four Egyptian Families
Established Conditions List (PDF)
FRAS1 Gene Fraser Extracellular Matrix Complex Subunit 1
Connective Tissue Disorders
Fraser Syndrome – a Case Report BEGUM SHARIFUN NAHER
Aase–Smith Syndrome, 231 Abboud, M.R., 381 Abdallat Syndrome, 196
The Molecular Basis of Human Anophthalmia and Microphthalmia
ORPHA Number Disease Or Group of Diseases 300305 11P15.4
Fraser Syndrome
Qgenomics Genomics for Human Health
Fraser Syndrome
First and Second Branchial Arch Syndromes: Multimodality Approach
UNILATERAL RENAL AGENESIS and the CONGENITAL SOLITARY FUNCTIONING KIDNEY WOOLF and HILLMAN
An Interesting Case of Fraser's Syndrome with Cryptophthalmos In
Fraser Syndrome and Cryptophthalmos: Review of the Diagnostic Criteria and Evidence for Phenotypic Modules in Complex Malformati
The Hidden Eye a Case of Cryptophthalmos Department of Ophthalmology and Visual Sciences University of the Philippines Philippine General Hospital Manila, Philippines
Autism and Attention Deficit Hyperactivity Disorder Precision Panel
Genetics for Obstetricians and Gynaecologists Chapter: Genetic Markers on Ultrasound Scan
11 CE AS-20689-Fraser Syndrome Case Report
Novel Insights Into the Pathogenesis of Monogenic Congenital Anomalies of the Kidney and Urinary Tract
Characterization of Deletions in a Cohort with Cleft Lip and Palate
Download Gene List
Craniofacial Anomalies and Associated Birth Defects
Prenatal Diagnosis of Fraser Syndrome Caused by Novel Variants
Mutation Analysis of the FRAS1 Gene Demonstrates New Mutations in a Propositus with Fraser Syndrome
A Practical Guide to the Management of Anophthalmia and Microphthalmia
Fraser Syndrome – a Dilemma to Parents
Mild Recessive Mutations in Six Fraser Syndrome– Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract
Established Conditions List
Supplemental Data
Prenatal Diagnosis of Fraser Syndrome