Literature DB >> 7853380

The possible Middle East origin of the mutation for the limb/pelvis-hypoplasia/aplasia syndrome.

M A Sabry.   

Abstract

Entities:  

Mesh：

Year:  1994        PMID： 7853380      PMCID： PMC1016673          DOI： 10.1136/jmg.31.11.897

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


× No keyword cloud information.
  4 in total

Review 1.  Pathological features and prenatal diagnosis in the newly recognised limb/pelvis-hypoplasia/aplasia syndrome.

Authors:  A Raas-Rothschild; R M Goodman; S Meyer; M B Katznelson; S T Winter; E Gross; M Tamarkin; T Ben-Ami; L Nebel; S Mashiach
Journal:  J Med Genet       Date:  1988-10       Impact factor: 6.318

2.  Profound limb deficiency, thoracic dystrophy, unusual facies, and normal intelligence: a new syndrome.

Authors:  S A Al-Awadi; A S Teebi; T I Farag; K M Naguib; M Y el-Khalifa
Journal:  J Med Genet       Date:  1985-02       Impact factor: 6.318

Review 3.  Limb/pelvis-hypoplasia/aplasia syndrome (Al-Awadi/Raas-Rothschild syndrome): report of two Italian sibs and further confirmation of autosomal recessive inheritance.

Authors:  G Camera; G Ferraiolo; D Leo; A Spaziale; S Pozzolo
Journal:  J Med Genet       Date:  1993-01       Impact factor: 6.318

Review 4.  The newly recognised limb/pelvis-hypoplasia/aplasia syndrome: report of a Bedouin patient and review.

Authors:  T I Farag; S A al-Awadi; M J Marafie; L Bastaki; S A al-Othman; F M Mohammed; I S AlSuliman; D S Murthy
Journal:  J Med Genet       Date:  1993-01       Impact factor: 6.318
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.