Literature DB >> 13444313

The coincidence of hemoglobin J and Fanconi's syndrome of hypoplastic anemia with hypoplasia of the spleen in a young man.

M E MCCABE, R D LANGE, W H CROSBY.   

Abstract

Entities:  

Keywords:  ANEMIA, APLASTIC/case reports; HEMOGLOBIN; SPLEEN/diseases

Mesh:

Substances:

Year:  1957        PMID: 13444313     DOI: 10.1016/0002-9343(57)90204-8

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


× No keyword cloud information.
  5 in total

1.  Sickle-cell/haemoglobin-J disease.

Authors:  L N WENT; J E MACIVER
Journal:  Br Med J       Date:  1959-08-08

2.  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

3.  Haemoglobin J in the French Canadian.

Authors:  S Kelly; L Desjardins; D Juckett
Journal:  J Med Genet       Date:  1970-12       Impact factor: 6.318

4.  [Fanconi anemia in an adult].

Authors:  G Perona; R Testolin
Journal:  Blut       Date:  1966-05

5.  Spectrum of anomalies in Fanconi anaemia.

Authors:  A Glanz; F C Fraser
Journal:  J Med Genet       Date:  1982-12       Impact factor: 6.318

  5 in total

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