Literature DB >> 8071951

The morbid anatomy of the human genome: chromosomal location of mutations causing disease (update 1 December 1993).

V A McKusick1, J S Amberger.   

Abstract

Entities:  

Mesh：

Year:  1994        PMID： 8071951      PMCID： PMC1049798          DOI： 10.1136/jmg.31.4.265

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


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  5 in total

Review 1.  Exploiting human anatomical variability as a link between genome and cognome.

Authors:  C M Leonard; M A Eckert; J M Kuldau
Journal:  Genes Brain Behav       Date:  2006       Impact factor: 3.449

Review 2.  From genes to public health: the applications of genetic technology in disease prevention. Genetics Working Group.

Authors:  M J Khoury
Journal:  Am J Public Health       Date:  1996-12       Impact factor: 9.308

3.  Myocardial infarction resulting from coronary artery dissection in an adolescent with Ehlers-Danlos syndrome type IV due to a type III collagen mutation.

Authors:  L C Adès; R D Waltham; A A Chiodo; J F Bateman
Journal:  Br Heart J       Date:  1995-08

Review 4.  A gene map of congenital malformations.

Authors:  A O Wilkie; J S Amberger; V A McKusick
Journal:  J Med Genet       Date:  1994-07       Impact factor: 6.318

5.  Screening of RET gene mutations in Chinese patients with medullary thyroid carcinoma and their relatives.

Authors:  Junyi Wang; Bin Zhang; Wensheng Liu; Yongxia Zhang; Xuebing Di; Yanmei Yang; Dangui Yan
Journal:  Fam Cancer       Date:  2016-01       Impact factor: 2.375
  5 in total

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