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Gillespie syndrome
Genes in Eyecare Geneseyedoc 3 W.M
Ophthalmology
WES Gene Package Multiple Congenital Anomalie.Xlsx
Orphanet Report Series Rare Diseases Collection
Mackenzie's Mission Gene & Condition List
Psykisk Utviklingshemming Og Forsinket Utvikling
The Effects of Physical Therapy Intervention on a 7 Month Old Child Diagnosed with Gillespie‟S Syndrome
Gillespie Syndrome in a South Asian Child
Genetic Background of Ataxia in Children Younger Than 5 Years in Finland E444
Early ACCESS Diagnosed Conditions List
A New Phenotype of Recessively Inherited Foveal Hypoplasia and Anterior Segment Dysgenesis Maps to a Locus on Chromosome 16Q23.2–24.2
Whole Exome Sequencing Gene Package Movement Disorders, Version 6.1, 31-1-2020
WES Gene Package Movement Disorders.Xlsx
Download CGT Exome V2.0
Ocular Manifestations of Inherited Diseases Maya Eibschitz-Tsimhoni
Utviklingsavvik V02
Whole Exome Sequencing Gene Package Multiple Congenital Anomaly, Version 8.1, 31-1-2020
Platform Abstracts
Top View
TEST CATALOGUE October 2020 ACHIEVING a POSITIVE CHANGE
WES Gene Package Intellectual Disability.Xlsx
Pax Genes: Regulators of Lineage Specification and Progenitor Cell Maintenance Judith A
Antibodies for Developmental Biology
Chromohelkosis May Underlie Chromosomal Instability and Mosaicism in Disease and Aging
Ataxia Genetic Testing 1
Mackenzie's Mission Gene & Condition List
The Genetic Nomenclature of Recessive Cerebellar Ataxias
Diagnoses Cue Sheet, P-00920
WES Gene Package Multiple Congenital Anomalie.Xlsx
Mendeliome Panel Versie V3 (4362 Genen) Centrum Voor Medische Genetica Gent
Mackenzie's Mission Gene & Condition List
An Approach to Integrating Exome Sequencing for Fetal Structural Anomalies Into Clinical Practice
Psykisk Utviklingshemming
Systemic Conditions with Ocular and Visual Manifestations
Individuals with Aniridia Or Gillespie Syndrome
WES Gene Package Multiple Congenital Anomalie
Type 1 Established Condition List
Supplementary Appendix For
Gillespie Syndrome in a South Asian Child: a Case Report With
Leistungsverzeichnis Der Sektion Pädiatrische Genetik Der Universitätskinderklinik Freiburg, Mathildenstr
List of Rare Diseases and Synonyms
Blueprint Genetics Microphthalmia, Anophthalmia and Anterior
OMIM Mendelian Gene List V2.0
A Novel Variant in PAX6 As the Cause of Aniridia in a Chinese Family
Genetic Diagnostics Test(S)/Gene(S)/Panel(S)