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Journal of Bone and Mineral Research

Volumn 16, Issue 12, 2001, Pages 2245-2250

Preonset studies of spondyloepiphyseal dysplasia tarda caused by a novel 2-base pair deletion in SEDL encoding sedlin

(5) Mumm, Steven a,b Zhang, Xiafang a Gottesman, Gary S b,c McAlister, William H d Whyte, Michael P a,b

a BARNES JEWISH HOSPITAL (United States)

b SHRINERS HOSPITAL FOR CHILDREN (United States)

c SAINT LOUIS UNIVERSITY SCHOOL OF MEDICINE (United States)

d ST LOUIS CHILDREN S HOSPITAL (United States)

Author keywords

Cartilage; Chondrocyte; Chondrodysplasia; Presymptomatic diagnosis; Rare splice site

Indexed keywords

PROTEIN; PROTEIN SEDL; SEDLIN; UNCLASSIFIED DRUG;

ADOLESCENT; ARTICLE; BASE PAIRING; CARTILAGE CELL; CASE REPORT; CHONDRODYSPLASIA; CLINICAL FEATURE; GENE DELETION; HUMAN; MALE; PATHOGENESIS; POLYMERASE CHAIN REACTION; SPINE RADIOGRAPHY; SPONDYLOEPIPHYSEAL DYSPLASIA;

ADOLESCENT; ADULT; BASE PAIRING; CARRIER PROTEINS; CHILD; CHILD, PRESCHOOL; EXONS; FEMALE; HUMANS; LUMBAR VERTEBRAE; MALE; MEMBRANE TRANSPORT PROTEINS; OSTEOCHONDRODYSPLASIAS; PEDIGREE; RNA, MESSENGER; SEQUENCE DELETION; SPINAL OSTEOPHYTOSIS; TRANSCRIPTION FACTORS;

EID: 0035196176 PISSN: 08840431 EISSN: None Source Type: Journal
DOI: 10.1359/jbmr.2001.16.12.2245 Document Type: Article

Times cited : (6)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.