Synpolydactyly
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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
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- 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