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Volumn 22, Issue 1, 2005, Pages 5-9
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HOXD13 polyalanine tract expansion in synpolydactyly: Mutation detection and prenatal diagnosis in a large Chinese family
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Author keywords
HOXD13 gene; Polyalanine expansion; Prenatal diagnosis; Synpolydactyly
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Indexed keywords
ALANINE;
GENOMIC DNA;
HOX PROTEIN;
HOXD13 PROTEIN;
PRIMER DNA;
UNCLASSIFIED DRUG;
AGAR GEL ELECTROPHORESIS;
ALLELE;
AMNION FLUID ANALYSIS;
ARTICLE;
BASE PAIRING;
BLOOD SAMPLING;
CHORION VILLUS SAMPLING;
CLINICAL ARTICLE;
CLINICAL FEATURE;
CLINODACTYLY;
CONTROLLED STUDY;
DIAGNOSTIC IMAGING;
DNA EXTRACTION;
DNA SEQUENCE;
DOMINANT INHERITANCE;
HAPLOTYPE;
HUMAN;
INTRON;
MICROSATELLITE MARKER;
NUCLEOTIDE REPEAT;
PHENOTYPE;
PHYSICAL EXAMINATION;
POLAND SYNDROME;
POLYMERASE CHAIN REACTION;
PRENATAL DIAGNOSIS;
SEQUENCE ANALYSIS;
BASE SEQUENCE;
CHINA;
DNA MUTATIONAL ANALYSIS;
FAMILY HEALTH;
FEMALE;
HOMEODOMAIN PROTEINS;
HUMANS;
MALE;
MOLECULAR SEQUENCE DATA;
MUTATION;
PEDIGREE;
PEPTIDES;
POLYDACTYLY;
POLYMERASE CHAIN REACTION;
PREGNANCY;
PRENATAL DIAGNOSIS;
TRANSCRIPTION FACTORS;
TRINUCLEOTIDE REPEAT EXPANSION;
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EID: 13544276985
PISSN: 10039406
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (7)
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References (6)
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