DOI: 10.1111/j.1365-2141.1958.tb03844.x. Hereditary Persistence of Foetal Haemoglobin Production, and its Interaction with the Sickle‐Cell Trait

Hereditary Persistence of Foetal Haemoglobin Production, and its Interaction with the Sickle‐Cell Trait

10.1111/j.1365-2141.1958.tb03844.x

Crossref journal-article

Wiley

British Journal of Haematology (311)

Bibliography

Jacob, G. F., & Raper, A. B. (1958). Hereditary Persistence of Foetal Haemoglobin Production, and its Interaction with the SickleâCell Trait. British Journal of Haematology, 4(2), 138â149. Portico.

Authors 2

Gillian F. Jacob (first)
Alan B. Raper (additional)

References 27 Referenced 61

10.1136/bmj.1.5021.734
10.1038/178857a0
10.1056/NEJM195508252530806
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10.1136/bmj.2.4951.1328
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10.1097/00005792-195605000-00002
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{'key': 'e_1_2_1_14_1', 'first-page': '517', 'article-title': 'Erythrocyte survival studies in childhood. II. Studies in Mediterranean anemia', 'volume': '36', 'author': 'KAPLAN E.', 'year': '1950', 'journal-title': 'J. Lab. clin. Med.'} / J. Lab. clin. Med. / Erythrocyte survival studies in childhood. II. Studies in Mediterranean anemia by KAPLAN E. (1950)
10.1182/blood.V9.9.897.897 / Blood / Paper electrophoresis of abnormal hemoglobins and its clinical applications. A simple semiquantitative method for the study of hereditary hemoglobinopathies by MOTULSKY A. G. (1954)
10.1126/science.110.2846.64
{'key': 'e_1_2_1_17_1', 'first-page': '138', 'article-title': 'Data on the occurrence of hemoglobin C and other abnormal hemoglobins in some African populations', 'volume': '8', 'author': 'NEEL J. V.', 'year': '1956', 'journal-title': 'Amer. J. hum. Genet.'} / Amer. J. hum. Genet. / Data on the occurrence of hemoglobin C and other abnormal hemoglobins in some African populations by NEEL J. V. (1956)
10.1126/science.110.2865.543
{'key': 'e_1_2_1_19_1', 'article-title': 'Thalassaemia in families of Indian origin', 'author': 'RAPER A. B.', 'year': '1958', 'journal-title': 'E. Afr. med. J.'} / E. Afr. med. J. / Thalassaemia in families of Indian origin by RAPER A. B. (1958)
{'issue': '2', 'key': 'e_1_2_1_20_1', 'article-title': 'Contributions to the modern knowledge of certain diseases of the blood', 'author': 'SILVESTRONI E.', 'year': '1951', 'journal-title': 'Sci. med. ital.'} / Sci. med. ital. / Contributions to the modern knowledge of certain diseases of the blood by SILVESTRONI E. (1951)
10.1016/0002-9343(55)90464-2
{'key': 'e_1_2_1_22_1', 'first-page': '193', 'article-title': 'Studies on abnormal hemoglobins. VII. The composition of the non‐S hemoglobin fraction in sickle‐cell anemia bloods. A comparative quantitative study by the method of electrophoresis and alkali denaturation', 'volume': '42', 'author': 'SINGER K.', 'year': '1953', 'journal-title': 'J. Lab. clin. Med.'} / J. Lab. clin. Med. / Studies on abnormal hemoglobins. VII. The composition of the non‐S hemoglobin fraction in sickle‐cell anemia bloods. A comparative quantitative study by the method of electrophoresis and alkali denaturation by SINGER K. (1953)
{'key': 'e_1_2_1_23_1', 'first-page': '405', 'article-title': 'Studies on abnormal hemoglobins. XI. Sickle‐cell‐thalassemia disease in the negro', 'volume': '10', 'author': 'SINGER K.', 'year': '1955', 'journal-title': 'Blood'} / Blood / Studies on abnormal hemoglobins. XI. Sickle‐cell‐thalassemia disease in the negro by SINGER K. (1955)
{'key': 'e_1_2_1_24_1', 'first-page': '289', 'article-title': 'Clinical features of the genetic variants of sickle cell disease', 'volume': '94', 'author': 'SMITH E. W.', 'year': '1954', 'journal-title': 'Bull. Johns Hopk. Hosp.'} / Bull. Johns Hopk. Hosp. / Clinical features of the genetic variants of sickle cell disease by SMITH E. W. (1954)
{'key': 'e_1_2_1_25_1', 'first-page': '763', 'article-title': "La tare thalassémique, chez les Bantous d'Afrique Centrale", 'volume': '36', 'author': 'STIJNS J.', 'year': '1956', 'journal-title': 'Ann. Soc. belg. Méd. trop.'} / Ann. Soc. belg. Méd. trop. / La tare thalassémique, chez les Bantous d'Afrique Centrale by STIJNS J. (1956)
10.1182/blood.V10.5.389.389 / Blood / Clinical manifestations of inherited abnormal hemoglobins. II. Interaction of hemoglobin‐E and thalassemia trait by STURGEON P. (1955)
{'key': 'e_1_2_1_27_1', 'first-page': '401', 'article-title': 'The natural history of homozygous sickle‐cell anaemia in Central Africa', 'volume': '26', 'author': 'TROWELL H. C.', 'year': '1957', 'journal-title': 'Quart. J. Med., N. S.'} / Quart. J. Med., N. S. / The natural history of homozygous sickle‐cell anaemia in Central Africa by TROWELL H. C. (1957)
{'key': 'e_1_2_1_28_1', 'first-page': '91', 'volume-title': 'Progress in Hematology', 'author': 'ZUELZER W. W.', 'year': '1956'} / Progress in Hematology by ZUELZER W. W. (1956)

Dates

Type	When
Created	17 years, 5 months ago (March 12, 2008, 11:34 a.m.)
Deposited	1 year, 9 months ago (Nov. 11, 2023, 11:58 a.m.)
Indexed	3 days, 2 hours ago (Sept. 4, 2025, 10 a.m.)
Issued	67 years, 5 months ago (April 1, 1958)
Published	67 years, 5 months ago (April 1, 1958)
Published Online	17 years, 5 months ago (March 12, 2008)
Published Print	67 years, 5 months ago (April 1, 1958)

Funders 0

None

BibTeX

@article{Jacob_1958, title={Hereditary Persistence of Foetal Haemoglobin Production, and its Interaction with the Sickle‐Cell Trait}, volume={4}, ISSN={1365-2141}, url={http://dx.doi.org/10.1111/j.1365-2141.1958.tb03844.x}, DOI={10.1111/j.1365-2141.1958.tb03844.x}, number={2}, journal={British Journal of Haematology}, publisher={Wiley}, author={Jacob, Gillian F. and Raper, Alan B.}, year={1958}, month=apr, pages={138–149} }

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