Literature DB >> 13493576

A new haemoglobin variant exhibiting anomalous electrophoretic behaviour.

R G SCHNEIDER, M E HAGGARD.   

Abstract

Keywords:  HEMOGLOBIN

Mesh：

Substances：

Year:  1957        PMID： 13493576     DOI： 10.1038/1801486a0

Source DB:  PubMed          Journal:  Nature        ISSN： 0028-0836            Impact factor:   49.962


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  7 in total

1.  A Swiss family with hemoglobin P Galveston beta117His leads to Arg, including two patients with hb P/beta thalassemia.

Authors:  E E Di Iorio; K H Winterhalter; K Wilson; A Rosenmund; H R Marti
Journal:  Blut       Date:  1975-08

2.  A critical review of human haemoglobin variants. II. Individual haemoglobins.

Authors:  G H BEAVEN; W B GRATZER
Journal:  J Clin Pathol       Date:  1959-03       Impact factor: 3.411

3.  PEPTIC ulcer in twins.

Authors: 
Journal:  Br Med J       Date:  1958-06-21

4.  Observations on some fast haemoglobins: K, J, N, and Bart's.

Authors:  J A AGER; H LEHMANN
Journal:  Br Med J       Date:  1958-04-19

5.  A haemoglobinopathy involving haemoglobin H and a new (Q) haemoglobin.

Authors:  F VELLA; R H WELLS; J A AGER; H LEHMANN
Journal:  Br Med J       Date:  1958-03-29

6.  Identification of mutation responsible for an enzyme polymorphism.

Authors:  J P Baker
Journal:  Biochem Genet       Date:  1978-12       Impact factor: 1.890

7.  Observations on haemoglobin P (Congo type).

Authors:  H Lehmann; D Charlesworth
Journal:  Biochem J       Date:  1970-10       Impact factor: 3.857
  7 in total

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