Next-generation sequencing for disorders of low and high bone mineral density

Osteoporosis International

Volumn 24, Issue 8, 2013, Pages 2253-2259

  Sule, G ^a   Campeau, P M ^a   Zhang, V W ^a   Nagamani, S C S ^a   Dawson, B C ^a   Grover, M ^a   Bacino, C A ^a   Sutton, V R ^a   Brunetti Pierri, N ^a,b,c   Lu, J T ^a   Lemire, E ^d   Gibbs, R A ^a   Cohn, D H ^e   Cui, H ^a   Wong, L J ^a   Lee, B H ^a,f  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b TELETHON INSTITUTE OF GENETICS AND MEDICINE TIGEM   (Italy)

^c UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^d UNIVERSITY OF SASKATCHEWAN   (Canada)

^e UNIVERSITY OF CALIFORNIA   (United States)

^f HOWARD HUGHES MEDICAL INSTITUTE   (United States)

Author keywords

High throughput; Molecular diagnosis; Next generation sequencing; Skeletal dysplasias

Indexed keywords

ALBERS SCHOENBERG DISEASE; ARTICLE; BONE DENSITY; CLINICAL ARTICLE; EHLERS DANLOS SYNDROME; EXON; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC SELECTION; HUMAN; MALE; MOLECULAR DIAGNOSIS; NUCLEOTIDE SEQUENCE; OSTEOGENESIS IMPERFECTA; PHENOTYPE; PRIORITY JOURNAL;

ADULT; BONE DENSITY; BONE DISEASES, DEVELOPMENTAL; EHLERS-DANLOS SYNDROME; GENE LIBRARY; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MALE; MUTATION; OSTEOGENESIS IMPERFECTA; OSTEOPETROSIS; SEQUENCE ANALYSIS, DNA;

EID: 84880311207     PISSN: 0937941X     EISSN: 14332965     Source Type: Journal    
DOI: 10.1007/s00198-013-2290-0     Document Type: Article

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