Literature DB >> 14187468

TWO UNRELATED PATIENTS WITH CONGENITAL CYANOSIS DUE TO HAEMOGLOBINOPATHY M.

M B FARMER, H LEHMANN, D N RAINE.   

Abstract

Entities:  

Keywords:  CHILD; CYANOSIS; GENETICS, HUMAN; HEART DISEASES; HEMOGLOBINS, ABNORMAL; METHEMOGLOBIN; SPECTROPHOTOMETRY

Mesh：

Substances：

Year:  1964        PMID： 14187468     DOI： 10.1016/s0140-6736(64)90563-x

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  5 in total

1.  HAEMOGLOBIN AND EVOLUTION.

Authors:  F L RAFFUCCI
Journal:  Br Med J       Date:  1965-09-18

2.  Myoglobin in primary muscular disease. I. Duchenne muscular dystrophy. II. Muscular dystrophy of distal type.

Authors:  A E Romero-Herrera; H Lehmann; B E Tomlinson; J N Walton
Journal:  J Med Genet       Date:  1973-12       Impact factor: 6.318

3.  De novo mutations producing unstable Hbs or Hbs M. II. Direct estimates of minimum nucleotide mutation rates in man.

Authors:  G Stamatoyannopoulos; P E Nute
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

4.  [HbM Hamburg, a beta chain anomaly: alpha-2-beta-2-63Tyr (equals HbM Saskatoon)].

Authors:  K Betke; E Kleihauer; R Gehring-Müller; G Braunitzer; J Jacobi; I Schmidt
Journal:  Klin Wochenschr       Date:  1966-08-15

5.  Structural and functional studies on hemoglobin Bethesda (alpha2beta2 145His), a varient associated with compensatory erythrocytosis.

Authors:  H F Bunn; T B Bradley; W E Davis; J W Drysdale; J F Burke; W S Beck; M B Laver
Journal:  J Clin Invest       Date:  1972-09       Impact factor: 14.808
  5 in total

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