Literature DB >> 5658391

Hereditary, X-linked, sideroachrestic anemia. The isolation of two erythrocyte populations differing in Xga blood type and porphyrin content.

G R Lee, W D MacDiarmid, G E Cartwright, M M Wintrobe.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1968        PMID： 5658391

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


× No keyword cloud information.
  9 in total

1.  Xg groups and sex abnormalities in people of northern European ancestry.

Authors:  R Sanger; P Tippett; J Gavin
Journal:  J Med Genet       Date:  1971-12       Impact factor: 6.318

2.  The X-linked blood group system Xg. Tests on unrelated people and families of northern European ancestry.

Authors:  R Sanger; P Tippett; J Gavin
Journal:  J Med Genet       Date:  1971-12       Impact factor: 6.318

3.  Genetics of protan and deutan color-vision anomalies: an instructive family.

Authors:  H C Thuline; W E Hodgkin; G R Fraser; A G Motulsky
Journal:  Am J Hum Genet       Date:  1969-11       Impact factor: 11.025

4.  X-chromosome inactivation and the Xg locus.

Authors:  P J Fialkow
Journal:  Am J Hum Genet       Date:  1970-07       Impact factor: 11.025

5.  X-linked sideroblastic anemia and ataxia: linkage to phosphoglycerate kinase at Xq13.

Authors:  W H Raskind; E Wijsman; R A Pagon; T C Cox; M J Bawden; B K May; T D Bird
Journal:  Am J Hum Genet       Date:  1991-02       Impact factor: 11.025

6.  Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorder.

Authors:  R A Pagon; T D Bird; J C Detter; I Pierce
Journal:  J Med Genet       Date:  1985-08       Impact factor: 6.318

7.  Sideroblastic anaemia. A review of seven paediatric cases.

Authors:  B C Hamel; E D Schretlen
Journal:  Eur J Pediatr       Date:  1982-03       Impact factor: 3.183

8.  5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemia.

Authors:  G R Sutherland; E Baker; D F Callen; V J Hyland; B K May; M J Bawden; H M Healy; I A Borthwick
Journal:  Am J Hum Genet       Date:  1988-09       Impact factor: 11.025

9.  The X-chromosomal human biglycan gene BGN is subject to X inactivation but is transcribed like an X-Y homologous gene.

Authors:  C Geerkens; U Vetter; W Just; N S Fedarko; L W Fisher; M F Young; J D Termine; P G Robey; D Wöhrle; W Vogel
Journal:  Hum Genet       Date:  1995-07       Impact factor: 4.132
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.