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Synpolydactyly
Type II Familial Synpolydactyly: Report on Two Families with an Emphasis on Variations of Expression
The Genetic Basis for Skeletal Diseases
Genetics of Congenital Hand Anomalies
Angeborene Fehlbildungen Der Extremitäten
Polydactyly of the Hand
Evolution of Morphology: Modifications to Size and Pattern
Congenital Malformations in Sea Turtles: Puzzling Interplay Between Genes and Environment
Review Article Cleidocranial Dysplasia: Clinical and Molecular Genetics
25. C:\Documents and Settings\Kwang-Il\My
Zur Morphologie Und Vererbung Des Polydaktylie-Luxations-Syndroms Bei Dem Wistar-Rattenstamm Shoe: WIST (Shoe)
Triplet Repeat Diseases
REVIEW ARTICLE Genetic Disorders of the Skeleton: a Developmental Approach
Genetic Screening of 202 Individuals with Congenital Limb Malformations
The Genomic and Clinical Landscape of Fetal Akinesia
Prenatal Microarray Disorders List V19.1
Congenital Hand Anomalies and Associated Syndromes Ghazi M
The Genetic Basis of Human Craniosynostosis Syndromes
Genomeposter2009.Pdf
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A Novel Duplication in the HOXA13 Gene in a Family with Atypical Hand-Foot-Genital Syndrome L Frisén, K Lagerstedt, M Tapper-Persson, I Kockum, a Nordenskjöld
(Synpolydactyly). 1 Field Investigation, Clinical and Pedigree Data J Med Genet: First Published As 10.1136/Jmg.32.6.421 on 1 June 1995
View Presentation Slides
Clinical and Genetic Examination of Limb Developmental Defects
Type a to Chromosome 7Pl 5-Qi 1.23 Bylinkage Analysis
Connective Tissue Disorders
Chromosomal Microarray Chromosomal Microarray
Intrinsic Disorder in Proteins with Pathogenic Repeat Expansions
Molecular and Clinical Analyses of Greig Cephalopolysyndactyly And
Congenital Malformations Notice
Microduplications Upstream of MSX2 Are Associated with a Phenocopy Of
Those Followed by F Indicate Figures
Angeborene Fehlbildungen A.-K
Book V2.Indb
Newborndxtm Advanced Sequencing Evaluation Disorders List
The Epidemiology, Genetics and Future Management of Syndactyly D
An Update on the Neurological Short Tandem Repeat Expansion Disorders and the Emergence of Long-Read Sequencing Diagnostics
List of Entries Essays Are Shown in Bold
Toe Ball Abnormality
Nosology and Classification of Genetic Skeletal Disorders: 2015 Revision
Screening of the ARX Gene in 682 Retarded Males
Limb Defects Sequencing Panel
WES Gene Package Multiple Congenital Anomalie
SPD) Pedigree
Table of Contents
Cleidocranial Dysplasia Spectrum Disorder
Synpolydactyly Phenotypes Correlate with Size of Expansions in HOXD13 Polyalanine Tract
In Split Handl Split Foot Malformation
Prenatal Chromosomal Analysis
Original Article Novel HOXD13 Frameshift Mutation Causes Synpolydactyly and Clinodactyly
Genetic Studies of Hypospadias
A Nonsense Mutation in the HOXD13 Gene Underlies Synpolydactyly with Incomplete Penetrance
OMIM Mendelian Gene List V2.0
Cleft Lip and Palate Precision Panel Overview Indications Clinical
Disease ID Disorder Name Gene Symbols OMIM ID