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Feingold syndrome
TARGETED GENE PANELS and REFERENCE SEQUENCE (Refseq) TRANSCRIPTS by PHENOTYPE
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Feingold Syndrome
Genetic Architecture for Human Aggression: a Study of Gene–Phenotype Relationship in OMIM Yanli Zhang-James1 and Stephen V
Congenital Hand Anomalies and Associated Syndromes Ghazi M
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Table of Contents
Orphanet Report Series 180 160 Collection 140 Rare Diseases
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De Novo GLI3 Mutation in Esophageal Atresia: Reproducing the Phenotypic Spectrum of Gli3 Defects in Murine Models
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TARGETED GENE PANELS and REFERENCE SEQUENCE (Refseq) TRANSCRIPTS by PHENOTYPE
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Disease ID Disorder Name Gene Symbols OMIM ID