Males with familial idiopathic scoliosis: A distinct phenotypic subgroup

Spine

Volumn 35, Issue 2, 2010, Pages 162-168

  Clough, Mark ^a   Justice, Cristina M ^b   Marosy, Beth ^a   Miller, Nancy H ^c  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b NATIONAL INSTITUTES OF HEALTH   (United States)

^c UNIVERSITY OF COLORADO   (United States)

Author keywords

Chromosome 17; Genomic screen; Idiopathic scoliosis; Linkage analysis

Indexed keywords

CARBOXYPEPTIDASE D; INDUCIBLE NITRIC OXIDE SYNTHASE; NEUROFIBROMIN; SEROTONIN TRANSPORTER;

ARTICLE; CHROMOSOME 17P; FAMILIAL IDIOPATHIC SCOLIOSIS; GENE; GENE IDENTIFICATION; GENE LOCUS; GENE MAPPING; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC SCREENING; GENETIC TRAIT; GENOME ANALYSIS; HUMAN; IDIOPATHIC SCOLIOSIS; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SPINE SURGERY;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; GENETIC ASSOCIATION STUDIES; GENETIC HETEROGENEITY; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; GENOTYPE; HUMANS; LINKAGE (GENETICS); MALE; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; SCOLIOSIS;

EID: 77749324004     PISSN: 03622436     EISSN: 15281159     Source Type: Journal    
DOI: 10.1097/BRS.0b013e3181b7f1a7     Document Type: Article

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