Literature DB >> 4753369

[Deletion of the short arm of chromosome 18 and trisomy 18 in a pair of siblings with unusual form of porphyria].

N Simon, J Hunyadi, A Szörényi, G Szemere.   

Abstract

Mesh:

Year:  1973        PMID: 4753369

Source DB:  PubMed          Journal:  Hautarzt        ISSN: 0017-8470            Impact factor:   0.751


× No keyword cloud information.
  2 in total

1.  18p-Mosaicism: case report and review.

Authors:  T Motegi; A Ichikawa; M Noda; G Hashimoto; M Kaga
Journal:  Hum Genet       Date:  1978-10-31       Impact factor: 4.132

2.  Erythropoietic protoporphyria, heterozygous cystinuria, and reduced peptidase A activity in a patient with 46,XX/46,XX,18q--mosaicism.

Authors:  E W Naylor; W H Murphey; E I Domoszlai; R Guthrie
Journal:  J Med Genet       Date:  1978-04       Impact factor: 6.318

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.