HETEROCELLULAR HEREDITARY PERSISTENT FETAL HEMOGLOBIN (HHPFH) OCCURRING IN SICKLE TRAIT (AS) PARENTS NOT CONSISTENTLY LINKED TO THE BETA-S (BETA-S) GENE IN OFFSPRING WITH HOMOZYGOUS SICKLE-CELL DISEASE (SS) OR TRAIT

被引：0
|
作者：
ABSHIRE, TC
ROLOFF, JS
WALKER, L
SELTZER, WK
JACKSON, T
MCCABE, ERB
GITHENS, JH
机构：
[1] CHILDRENS HOSP,DENVER,CO 80218
[2] UNIV COLORADO,HLTH SCI CTR,DEPT PEDIAT,DENVER,CO 80262
来源：
CLINICAL RESEARCH | 1987年 / 35卷 / 01期
关键词：
D O I：
暂无
中图分类号：
R-3 [医学研究方法]; R3 [基础医学];
学科分类号：
1001 ;
摘要：
引用
收藏
页码：A210 / A210
页数：1
相关论文
共 15 条
  • [1] FETAL HEMOGLOBIN LEVELS AND BETA-S GLOBIN HAPLOTYPES IN AN INDIAN POPULATION WITH SICKLE-CELL DISEASE
    KULOZIK, AE
    KAR, BC
    SATAPATHY, RK
    SERJEANT, BE
    SERJEANT, GR
    WEATHERALL, DJ
    BLOOD, 1987, 69 (06) : 1742 - 1746
  • [2] BETA-S CHAIN TURNOVER IN RETICULOCYTES OF SICKLE TRAIT INDIVIDUALS WITH HIGH OR LOW CONCENTRATIONS OF HEMOGLOBIN-S
    SHAEFFER, JR
    KLEVE, LJ
    DESIMONE, J
    BRITISH JOURNAL OF HAEMATOLOGY, 1976, 32 (03) : 365 - 372
  • [3] BETA+-THALASSEMIA IN CIS OF A SICKLE-CELL GENE - OCCURRENCE OF A PROMOTER MUTATION ON A BETA-S CHROMOSOME
    BAKLOUTI, F
    OUAZANA, R
    GONNET, C
    LAPILLONNE, A
    DELAUNAY, J
    GODET, J
    BLOOD, 1989, 74 (05) : 1817 - 1822
  • [4] RELATIONSHIP OF FETAL HEMOGLOBIN LEVELS AND BETA-S-HAPLOTYPES IN HOMOZYGOUS SICKLE-CELL DISEASE
    FALUSI, AG
    KULOZIK, AE
    EUROPEAN JOURNAL OF HAEMATOLOGY, 1990, 45 (01) : 1 - 4
  • [5] PREFERENTIAL BINDING OF BETA-S GLOBIN CHAINS ASSOCIATED WITH STROMA IN SICKLE-CELL DISORDERS
    BANK, A
    MEARS, G
    WEISS, R
    ODONNELL, JV
    NATTA, C
    JOURNAL OF CLINICAL INVESTIGATION, 1974, 54 (04): : 805 - 809
  • [6] ANALYSIS OF GENE DOSAGE OF SICKLE-CELL BETA-GLOBIN (BETA-S) IN HUMAN GENOMIC DNA BY DNA HYBRIDIZATION WITH SYNTHETIC OLIGONUCLEOTIDES
    CONNER, B
    WALLACE, RB
    TEPLITZ, RL
    CLINICAL RESEARCH, 1982, 30 (01): : A46 - A46
  • [7] SICKLE-CELL DISEASE IN A PATIENT WITH SICKLE-CELL TRAIT AND COMPOUND HETEROZYGOSITY FOR HEMOGLOBIN-S AND HEMOGLOBIN QUEBEC-CHORI
    WITKOWSKA, HE
    LUBIN, BH
    BEUZARD, Y
    BARUCHEL, S
    ESSELTINE, DW
    VICHINSKY, EP
    KLEMAN, KM
    BARDAKDJIANMICHAU, J
    PINKOSKI, L
    CAHN, S
    ROITMAN, E
    GREEN, BN
    FALICK, AM
    SHACKLETON, CHL
    NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (16): : 1150 - 1154
  • [8] INCREASED HBF IN SICKLE-CELL-ANEMIA IS DETERMINED BY A FACTOR LINKED TO THE BETA-S GENE FROM ONE PARENT
    MILNER, PF
    LEIBFARTH, JD
    FORD, J
    BARTON, BP
    GRENETT, HE
    GARVER, FA
    BLOOD, 1984, 63 (01) : 64 - 72
  • [9] BETA-S GENE-CLUSTER HAPLOTYPES MODULATE HEMATOLOGIC AND HEMORHEOLOGIC EXPRESSION IN SICKLE-CELL-ANEMIA - USE IN PREDICTING CLINICAL SEVERITY
    POWARS, DR
    MEISELMAN, HJ
    FISHER, TC
    HITI, A
    JOHNSON, C
    AMERICAN JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 1994, 16 (01): : 55 - 61
  • [10] BETA-THALASSAEMIA, HEMOGLOBIN S AND HEREDITARY ELLIPTOCYTOSIS IN A ZAIRIAN FAMILY - ISCHEMIC COSTAL NECROSES IN A CHILD WITH SICKLE-CELL BETA-THALASSAEMIA
    VANROS, G
    SEYNHAEVE, V
    FIASSE, L
    ACTA HAEMATOLOGICA, 1976, 56 (04) : 241 - 252
12