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

Access to Document

10.3109/03630268709042859

Fingerprint Dive into the research topics of 'HB p-nilotic or α<sub>2</sub>(βdelta;<sub>2</sub> in a turkish family'. Together they form a unique fingerprint.

Cite this

@article{61ec4fbcf0cb4c41a0e765e6adcc1a7d,

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",

number = "4",

}

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.

UR - http://www.scopus.com/inward/record.url?scp=0023076155&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0023076155&partnerID=8YFLogxK

U2 - 10.3109/03630268709042859

DO - 10.3109/03630268709042859

M3 - Article

C2 - 3667326

AN - SCOPUS:0023076155

VL - 11

SP - 395

EP - 399

JO - Hemoglobin

JF - Hemoglobin

SN - 0363-0269

IS - 4