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Heterozygote expression in Grebe Chondrodysplasia

  • Published:2008-04-23 Issue:5 Volume:29 Page:455-456
  • ISSN:0009-9163
  • Container-title:Clinical Genetics
  • language:en
  • Short-container-title:

Author:

Curtis Diana

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference5 articles.

1. A kindred of Miao Nationality affected with Grebe-Quelco-Salgado Achondrogenesis.;Feng;Acta Genet. Sinica,1985

2. Non-lethal achondrogenesis (Grebe-Quelco- Salgado type) in two Puerto Rican sibships.;Garcia-Castro;J. Paediatr.,1975

3. Grebe Chondrodysplasia and brachydactyly in a family.;Kumar;Clin. Genet.,1984

4. A new type of dwarfism with various bone aplasias and hypoplasias of the extremities.;Quelco-Salgado;Acta Genet. (Basel),1964

5. A rare genetic syndrome.;Quelco-Salgado;Lancet,1968

Cited by 13 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. Homozygous missense and nonsense mutations in BMPR1B cause acromesomelic chondrodysplasia-type Grebe;European Journal of Human Genetics;2013-10-16

2. Grebe-type chondrodysplasia: a novel missense mutation in a conserved cysteine of the growth differentiation factor 5;Journal of Bone and Mineral Metabolism;2008-11

3. THE FETAL MUSCULOSKELETAL SYSTEM;Ultrasonography in Obstetrics and Gynecology;2008

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

5. Clinical and molecular analysis of Grebe acromesomelic dysplasia in an Omani family;American Journal of Medical Genetics;2003-07-30
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