Beryl E. Serjeant researcher
Serjeant, Beryl E.
VIAF ID: 58583003 (Personal)
Permalink: http://viaf.org/viaf/58583003
Preferred Forms
- 100 0 _ ‡a Beryl E. Serjeant ‡c researcher
- 100 1 _ ‡a Serjeant, Beryl E.
- 100 1 _ ‡a Serjeant, Beryl E.
- 100 1 _ ‡a Serjeant, Beryl E.
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- 100 1 _ ‡a Serjeant, Beryl E.
-
4xx's: Alternate Name Forms (2)
5xx's: Related Names (1)
Works
Title | Sources |
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The clinical features of sickle-cell- thalassaemia in Jamaica. | |
A comparison of sickle cell syndromes in Northern Greece | |
The conjunctival sign in sickle cell anemia. A relationship with irreversibly sickled cells | |
Counselling mothers of babies with the sickle cell trait: to be or not to be | |
Early rise in the "pitted" red cell count as a guide to susceptibility to infection in childhood sickle cell anaemia | |
Haematological indices in normal negro children: a Jamaican cohort from birth to five years. | |
Haemoglobin caribbean beta91 (F7) Leu replaced by Arg: a mildly haemoglobin with a low oxygen affinity | |
Haemoglobin F Victoria Jubilee (alpha 2 A gamma 2 80 Asp-Try). | |
Haemoglobin gene frequencies in the Jamaican population: a study in 100,000 newborns | |
Haemoglobin Spanish Town alpha27 Glu replaced by Val (B8) | |
Haemoglobin Variant Screening in Jamaica: Meeting Student's Request. | |
Hb F Kingston (G gamma 55 [D6] Met leads to Arg) | |
HB S-HB Monroe; a sickle cell-beta-thalassemia syndrome | |
Hb S-β-thalassemia: molecular, hematological and clinical comparisons. | |
Heights and weights of West Indian children with the sickle cell trait | |
Hurricane Gilbert anaemia | |
The in vivo sickle phenomenon: a reappraisal. | |
Inadequacy of Hb Bart's as an indicator of alpha thalassaemia | |
Interaction of the alpha alpha alpha globin gene haplotype and sickle haemoglobin | |
Iron Deficiency among Jamaican Adolescents | |
Jamaican Sbeta+-thalassaemia: mutations and haematology | |
Microchromatographic quantitation of hemoglobin A levels in phenotypes of sickle cell-beta(+) thalassemia | |
The molecular basis of alpha thalassemia in India. Its interaction with the sickle cell gene | |
Neonatal screening for sickle hemoglobin | |
Oral zinc sulphate treatment of chronic non-sickle cell ulcers in Jamaica | |
Outbreak of aplastic crises in sickle cell anaemia associated with parvovirus-like agent | |
Plasma proteins in children with trichuris dysentery syndrome | |
Screening for the beta-thalassaemia trait: hazards among populations of West African Ancestry | |
Sickle-cell anaemia before Herrick. | |
Sickle cell disease, 2001: | |
Sickle cell-hereditary persistence of fetal haemoglobin and its differentiation from other sickle cell syndromes | |
A simple micromethod for the measurement of fetal haemoglobin | |
A whole blood solubility and centrifugation test for sickle cell hemoglobin: a clinical trial | |
β-Thalassemia Mutations in Jamaica: Geographic Variation in Small Communities |