Evidence for locus heterogeneity in the Camurati-Engelmann (DPD1) Syndrome [1]

Clinical Genetics

Volumn 59, Issue 3, 2001, Pages 198-200

  Hecht, Jacqueline T ^a,b   Blanton, Susan H ^c   Broussard, Sherrice ^a   Scott, Allison ^b   Hall, Catherine Rhoades ^a   Milunsky, Jeff M ^d  

^a UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

^b Shriners Hospital for Children in Houston   (United States)

^c UNIVERSITY OF VIRGINIA   (United States)

^d BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSFORMING GROWTH FACTOR BETA1;

AUTOSOMAL DOMINANT DISORDER; BONE DISEASE; BONE PAIN; BONE RADIOGRAPHY; CAMURATI ENGELMANN SYNDROME; CHROMOSOME 19Q; CHROMOSOME MAP; CHROMOSOME MARKER; CLINICAL ARTICLE; DIAPHYSIS; FATIGUE; FEMALE; GAIT DISORDER; GENE LOCUS; GENE MUTATION; GENETIC ANALYSIS; GENETIC HETEROGENEITY; GENETIC LINKAGE; HUMAN; HUMAN TISSUE; LETTER; LONG BONE; MALE; MUSCLE WEAKNESS; OSTEOSCLEROSIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SKULL; WASTING SYNDROME;

ADULT; CAMURATI-ENGELMANN SYNDROME; CHILD; FEMALE; GENETIC HETEROGENEITY; HUMANS; LINKAGE (GENETICS); MALE; PEDIGREE; TRANSFORMING GROWTH FACTOR BETA; TRANSFORMING GROWTH FACTOR BETA1;

EID: 0035096372     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2001.590310.x     Document Type: Letter

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