Literature DB >> 20788973

Haemoglobin O in An Arab Family.

B Ramot, S Fisher, D Remez, R Schneerson, D Kahane, J A Ager, H Lehmann.   

Abstract

Year:  1960        PMID： 20788973      PMCID： PMC2097055          DOI： 10.1136/bmj.2.5208.1262

Source DB:  PubMed          Journal:  Br Med J        ISSN： 0007-1447


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  7 in total

1.  Chemistry of the abnormal human haemoglobins.

Authors:  V M INGRAM
Journal:  Br Med Bull       Date:  1959-01       Impact factor: 4.291

2.  Haemoglobin P in a family in the Belgian Congo.

Authors:  P DHERTE; H LEHMANN; J VANDEPITTE
Journal:  Nature       Date:  1959-10-10       Impact factor: 49.962

3.  Blood groups, haemoglobins, and thalassaemia in Turks in southern Turkey and Eti-Turks.

Authors:  M AKSOY; E W IKIN; A E MOURANT; H LEHMANN
Journal:  Br Med J       Date:  1958-10-18

4.  Formation of normal and doubly abnormal haemoglobins by recombination of haemoglobin I with S and C.

Authors:  H A ITANO; E ROBINSON
Journal:  Nature       Date:  1959-06-27       Impact factor: 49.962

5.  Haemoglobin O (Buginese X) in Sulawesi.

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

6.  Study of two abnormal hemoglobins with evidence for a new genetic locus for hemoglobin formation.

Authors:  E W SMITH; J V TORBERT
Journal:  Bull Johns Hopkins Hosp       Date:  1958-01

7.  Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.

Authors:  K SINGER; A I CHERNOFF; L SINGER
Journal:  Blood       Date:  1951-05       Impact factor: 22.113
  7 in total
  5 in total

1.  SICKLE-CELL HAEMOGLOBIN K DISEASE.

Authors:  P O GORMAN; K M ALLSOPP; H LEHMANN; P K SUKUMARAN
Journal:  Br Med J       Date:  1963-11-30

2.  Twelve families with Hb O Arab in the Burgas district of Bulgaria. Observations on sixteen examples of Hb O Arab-beta (0) thalassaemia.

Authors:  K N Kantchev; B N Tcholakov; R Casey; H Lehmann; M El Hazmi
Journal:  Humangenetik       Date:  1975

3.  Homozygous haemoglobin O disease and conjugated hyperbilirubinaemia in a Sudanese family.

Authors:  S A Ibrahim; D Mustafa; A O Mohamed; M B Mohed
Journal:  BMJ       Date:  1992-01-04

4.  Survey on haemoglobin variants, beta thalassaemia, glucose-6-phosphate dehydrogenase deficiency, and haptoglobin types in Turks from western Thrace.

Authors:  M Aksoy; A Kutlar; F Kutlar; G Dinçol; S Erdem; S Baştesbihçi
Journal:  J Med Genet       Date:  1985-08       Impact factor: 6.318

5.  The interaction of hemoglobin O Arab with Hb S and beta+ thalassemia among Israeli Arabs.

Authors:  E A Rachmilewitz; H Tamari; F Liff; Y Ueda; R L Nagel
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132
  5 in total

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