HB p-nilotic or α2(βdelta;2 in a turkish family

C. Altay; A. Kutlar; J. B. Wilson; B. B. Webber; T. H.J. Huisman

doi:10.3109/03630268709042859

HB p-nilotic or α₂(βdelta;₂ in a turkish family

C. Altay, A. Kutlar, J. B. Wilson, B. B. Webber, T. H.J. Huisman

Pulmonary Disease

Research output: Contribution to journal › Article › peer-review

7 Scopus citations

Abstract

We recently examined a 16-year-old high school student who participated in a survey for Hemoglobinopathies in an Anatolian city in Turkey. Analysis if his hemoglobin (Hb) showed the presence of an electrophoretically slow-moving variant (at pH 8.6, about as Hb S) which, upon further examination, was also seen in his father, one brother, and one sister.

Original language	English (US)
Pages (from-to)	395-399
Number of pages	5
Journal	Hemoglobin
Volume	11
Issue number	4
DOIs	https://doi.org/10.3109/03630268709042859
State	Published - 1987

ASJC Scopus subject areas

Hematology
Clinical Biochemistry
Genetics(clinical)
Biochemistry, medical

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title = "HB p-nilotic or α2(βdelta;2 in a turkish family",

abstract = "We recently examined a 16-year-old high school student who participated in a survey for Hemoglobinopathies in an Anatolian city in Turkey. Analysis if his hemoglobin (Hb) showed the presence of an electrophoretically slow-moving variant (at pH 8.6, about as Hb S) which, upon further examination, was also seen in his father, one brother, and one sister.",

author = "C. Altay and A. Kutlar and Wilson, {J. B.} and Webber, {B. B.} and Huisman, {T. H.J.}",

note = "Funding Information: This investigation was supported i n part by the Turkish Scient i f i c and Technical Research Foundation, and i n part by USPHS Research Grants HLB-05168 and HLB-15158. This i s contribution #lo17 from the Department of Cell and Molecular Biology at the Medical College o f Georgia i n Augusta, Georgia.",

year = "1987",

doi = "10.3109/03630268709042859",

language = "English (US)",

volume = "11",

pages = "395--399",

journal = "Hemoglobin",

issn = "0363-0269",

publisher = "Informa Healthcare",

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TY - JOUR

T1 - HB p-nilotic or α2(βdelta;2 in a turkish family

AU - Altay, C.

AU - Kutlar, A.

AU - Wilson, J. B.

AU - Webber, B. B.

AU - Huisman, T. H.J.

N1 - Funding Information: This investigation was supported i n part by the Turkish Scient i f i c and Technical Research Foundation, and i n part by USPHS Research Grants HLB-05168 and HLB-15158. This i s contribution #lo17 from the Department of Cell and Molecular Biology at the Medical College o f Georgia i n Augusta, Georgia.

PY - 1987

Y1 - 1987

N2 - We recently examined a 16-year-old high school student who participated in a survey for Hemoglobinopathies in an Anatolian city in Turkey. Analysis if his hemoglobin (Hb) showed the presence of an electrophoretically slow-moving variant (at pH 8.6, about as Hb S) which, upon further examination, was also seen in his father, one brother, and one sister.

AB - We recently examined a 16-year-old high school student who participated in a survey for Hemoglobinopathies in an Anatolian city in Turkey. Analysis if his hemoglobin (Hb) showed the presence of an electrophoretically slow-moving variant (at pH 8.6, about as Hb S) which, upon further examination, was also seen in his father, one brother, and one sister.

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DO - 10.3109/03630268709042859

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C2 - 3667326

AN - SCOPUS:0023076155

VL - 11

SP - 395

EP - 399

JO - Hemoglobin

JF - Hemoglobin

SN - 0363-0269

IS - 4

ER -

HB p-nilotic or α₂(βdelta;₂ in a turkish family

Abstract

ASJC Scopus subject areas

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