Evidence for locus heterogeneity in the Camurati-Engelmann (DPD1) syndrome

Journal article

Peer reviewed

Jacqueline T HECHT, Susan H BLANTON, Sherrice BROUSSARD, Allison SCOTT, Catherine Rhoades HALL and Jeff M MILUNSKY

Clinical genetics, Vol.59(3), pp.198-200

2001

PMID: 11260231

Abstract

Biological and medical sciences

Medical sciences

Diseases of the osteoarticular system

Malformations and congenital and or hereditary diseases involving bones. Joint deformations

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Citation topics: 1 Clinical & Life Sciences; 1.80 Bone Diseases; 1.80.766 Osteoclast
Web Of Science research areas: Genetics & Heredity
ESI research areas: Clinical Medicine

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Source: InCites

Title: Evidence for locus heterogeneity in the Camurati-Engelmann (DPD1) syndrome
Creators: Jacqueline T HECHT - Department of Pediatrics, 6431 Fannin St, STE 3.136, Houston, TX 77030, United States
Susan H BLANTON - Department of Pediatrics, 6431 Fannin St, STE 3.136, Houston, TX 77030, United States
Sherrice BROUSSARD - Department of Pediatrics, 6431 Fannin St, STE 3.136, Houston, TX 77030, United States
Allison SCOTT - Department of Pediatrics, 6431 Fannin St, STE 3.136, Houston, TX 77030, United States
Catherine Rhoades HALL - Department of Pediatrics, 6431 Fannin St, STE 3.136, Houston, TX 77030, United States
Jeff M MILUNSKY - Department of Pediatrics, 6431 Fannin St, STE 3.136, Houston, TX 77030, United States
Publication Details: Clinical genetics, Vol.59(3), pp.198-200
Publisher: Blackwell
Academic Unit: Miller School of Medicine; John P. Hussman Institute for Human Genomics; UMMG Dept of Human Genetics (Dr. John T. Macdonald Foundation)
Language: English
Resource Type: Journal article
PMID: 11260231
Record Identifier: 991031597867702976