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Volumn 49, Issue 3, 1999, Pages 129-132

Localization of the gene responsible for familial benign polycythemia to chromosome 11q23

Author keywords

Chromosome 11q23; Erythrocytosis; Familial benign polycythemia; Linkage

Indexed keywords

ERYTHROPOIETIN; ERYTHROPOIETIN RECEPTOR; URIC ACID;

EID: 0032976810     PISSN: 00015652     EISSN: None     Source Type: Journal    
DOI: 10.1159/000022859     Document Type: Article
Times cited : (10)

References (15)
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  • 2
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    • Hemoglobin olympia (beta 20 valine to methionine): An electrophoretically silent variant associated with high oxygen affinity and erythrocytosis
    • Stamatoyannopoulos G, Nute PE, Adamson JW, Bellingham AJ, Funk D, Hornung S: Hemoglobin Olympia (beta 20 valine to methionine): An electrophoretically silent variant associated with high oxygen affinity and erythrocytosis. J Clin Invest 1973;52:342-349.
    • (1973) J Clin Invest , vol.52 , pp. 342-349
    • Stamatoyannopoulos, G.1    Nute, P.E.2    Adamson, J.W.3    Bellingham, A.J.4    Funk, D.5    Hornung, S.6
  • 6
    • 0015622182 scopus 로고
    • Recessive familial erythrocytosis: Aspects of marrow regulation in two families
    • Adamson JW, Stamatoyannopoulos G, Kontras S, Lascari A, Detter J: Recessive familial erythrocytosis: Aspects of marrow regulation in two families. Blood 1973;41:641-665.
    • (1973) Blood , vol.41 , pp. 641-665
    • Adamson, J.W.1    Stamatoyannopoulos, G.2    Kontras, S.3    Lascari, A.4    Detter, J.5
  • 7
    • 0018864180 scopus 로고
    • Congenital erythrocytosis: A new form, associated with an erythropoietin-dependent mechanism
    • Whitcomb WH, Peschle C, Moore M, Nitschke R, Adamson JW: Congenital erythrocytosis: A new form, associated with an erythropoietin-dependent mechanism. Br J Haematol 1980; 44:17-24.
    • (1980) Br J Haematol , vol.44 , pp. 17-24
    • Whitcomb, W.H.1    Peschle, C.2    Moore, M.3    Nitschke, R.4    Adamson, J.W.5
  • 8
    • 0016118725 scopus 로고
    • Familial erythrocytosis among inhabitants of the Chuvash ASSR
    • Polyakova LA: Familial erythrocytosis among inhabitants of the Chuvash ASSR (in Russian). Probl Gematol 1974;10:30-32.
    • (1974) Probl Gematol , vol.10 , pp. 30-32
    • Polyakova, L.A.1
  • 10
    • 0027202447 scopus 로고
    • A highly polymorphic (ACT)n VNTR (variable nucleotide of tandem repeats) locus inside intron 12 of COL1A2, one of the two genes involved in dominant osteogenesis imperfecta
    • Pepe G: A highly polymorphic (ACT)n VNTR (variable nucleotide of tandem repeats) locus inside intron 12 of COL1A2, one of the two genes involved in dominant osteogenesis imperfecta. Hum Mutat 1993;2:300-305.
    • (1993) Hum Mutat , vol.2 , pp. 300-305
    • Pepe, G.1
  • 11
    • 0025758289 scopus 로고
    • Refinement of human chromosome 7 map around the pro alpha 2 (I) collagen gene by long-range restriction mapping
    • Kere J, Tolvanen R, Donis Keller H, de la Chapelle A: Refinement of human chromosome 7 map around the pro alpha 2 (I) collagen gene by long-range restriction mapping. Nucl Acids Res 1991;19:2755-2759.
    • (1991) Nucl Acids Res , vol.19 , pp. 2755-2759
    • Kere, J.1    Tolvanen, R.2    Donis Keller, H.3    De La Chapelle, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.