Spondylar dysplasia (SD)/brachyolmia (BO), type I: search for qualitative anomalies in glycosaminoglycans (GAG)

Author:

Toledo Sergio P. A.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference11 articles.

1. La dysplasie spondylaire pure: un brachyolmie;Fontaine;Arch Fr Pediatr,1975

2. Brachyolmia, Hobaek type. A clinical, radiologic and histologic study;Horton;Am J Med Genet,1983

3. Absence of proteoglycan core protein in cartilage from the cmd/cmd (Cartilage matrix protein) mouse;Kimata;J Biol Chem,1981

4. Maroteaux P. Spondyloepiphyseal dysplasias and metatropic dwarfism. Birth Defects: Original Artical Series, 1st conference on the clinical delineation of Birth Defects. Part IV. Skeletal dysplasia National Foundation March of Dimes 1969 34 40

5. Excretion of chondroitin sulfate C with low sulfate content by patients with generalized platyspondyly(brachyolmia);Mourão;Biochem Med,1973

Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. B;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

2. Brachyolmia and spinal stenosis;American Journal of Medical Genetics;2003-06-23

3. Two sibs with brachyolmia type Hobaek: Five year follow-up through puberty;American Journal of Medical Genetics;2002-12-10

4. Membrane Receptor–Linked Disease States;Comprehensive Physiology;1998-12

5. Toledo type brachyolmia.;Archives of Disease in Childhood;1996-02-01

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