메뉴 건너뛰기




Volumn 61, Issue 2, 1997, Pages 458-461

Nonrandom X-chromosome inactivation in hemopoietic cells from carriers of dyskeratosis congenita [4]

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; CHILD; CHROMOSOME XQ; CLINICAL ARTICLE; CONTROLLED STUDY; DYSKERATOSIS CONGENITA; FEMALE; HEMATOPOIETIC CELL; HETEROZYGOTE; HUMAN; LETTER; PEDIGREE; PRIORITY JOURNAL; SCHOOL CHILD; X CHROMOSOME INACTIVATION;

EID: 0030826640     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0002-9297(07)64075-0     Document Type: Letter
Times cited : (19)

References (17)
  • 1
    • 0026678490 scopus 로고
    • Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation
    • RC Allen HY Zoghbi AB Moseley HM Rosenblatt JW Belmont Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation Am J Hum Genet 51 1992 1229 1239
    • (1992) Am J Hum Genet , vol.51 , pp. 1229-1239
    • Allen, RC1    Zoghbi, HY2    Moseley, AB3    Rosenblatt, HM4    Belmont, JW5
  • 2
    • 0027216789 scopus 로고
    • keratosis congenita: three additional families show linkage to a locus in Xq28
    • R Arngrimsson I Dokal L Luzzatto JM Connor keratosis congenita: three additional families show linkage to a locus in Xq28 J Med Genet 30 1993 618 619
    • (1993) J Med Genet , vol.30 , pp. 618-619
    • Arngrimsson, R1    Dokal, I2    Luzzatto, L3    Connor, JM4
  • 3
    • 0029885015 scopus 로고    scopus 로고
    • Genetic control of X inactivation and processes leading to X-inactivation skewing
    • JW Belmont Genetic control of X inactivation and processes leading to X-inactivation skewing Am J Hum Genet 58 1996 1101 1108
    • (1996) Am J Hum Genet , vol.58 , pp. 1101-1108
    • Belmont, JW1
  • 4
    • 0029901946 scopus 로고    scopus 로고
    • Nonrandom X-inactivation patterns in normal females: lyonization ratios vary with age
    • L Busque R Mio J Mattioli E Brais N Blais Y Lalonde M Maragh Nonrandom X-inactivation patterns in normal females: lyonization ratios vary with age Blood 88 1996 59 65
    • (1996) Blood , vol.88 , pp. 59-65
    • Busque, L1    Mio, R2    Mattioli, J3    Brais, E4    Blais, N5    Lalonde, Y6    Maragh, M7
  • 6
    • 0022477628 scopus 로고
    • Assignment of the gene for dyskeratosis congenita to Xq28
    • JM Connor D Gatherer FC Gray L Pirrit NA Affara Assignment of the gene for dyskeratosis congenita to Xq28 Hum Genet 72 1986 348 351
    • (1986) Hum Genet , vol.72 , pp. 348-351
    • Connor, JM1    Gatherer, D2    Gray, FC3    Pirrit, L4    Affara, NA5
  • 8
    • 0030097639 scopus 로고    scopus 로고
    • Dyskeratosis congenita: an inherited bone marrow failure syndrome
    • I Dokal Dyskeratosis congenita: an inherited bone marrow failure syndrome Br J Haematol 92 1996 775 779
    • (1996) Br J Haematol , vol.92 , pp. 775-779
    • Dokal, I1
  • 9
    • 0031016549 scopus 로고    scopus 로고
    • Polyclonal origin of medullary carcinoma of the thyroid in multiple endocrine neoplasia type 2
    • AM Ferraris R Mangerini GF Gaetani C Romei A Pinchera F Pacini Polyclonal origin of medullary carcinoma of the thyroid in multiple endocrine neoplasia type 2 Hum Genet 99 1997 202 205
    • (1997) Hum Genet , vol.99 , pp. 202-205
    • Ferraris, AM1    Mangerini, R2    Gaetani, GF3    Romei, C4    Pinchera, A5    Pacini, F6
  • 11
    • 0018906286 scopus 로고
    • Allelic exclusion of glucose-6-phosphate dehydrogenase in platelets and T lymphocytes from a Wiskott-Aldrich syndrome carrier
    • WJ Gealy JM Dwyer JB Harley Allelic exclusion of glucose-6-phosphate dehydrogenase in platelets and T lymphocytes from a Wiskott-Aldrich syndrome carrier Lancet 8159 1980 63 65
    • (1980) Lancet , vol.8159 , pp. 63-65
    • Gealy, WJ1    Dwyer, JM2    Harley, JB3
  • 16
    • 0023188706 scopus 로고
    • Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation
    • JM Puck RL Nussbaum ME Conley Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation J Clin Invest 79 1987 1395 1400
    • (1987) J Clin Invest , vol.79 , pp. 1395-1400
    • Puck, JM1    Nussbaum, RL2    Conley, ME3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.