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Rothmund-Thomson综合征1例 被引量:2

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摘要 Rothmund-Thomson综合征(即先天性皮肤异色症)是一种较少见的常染色体隐性遗传性疾病,至2001年止,全世界累计报告200余例,现报告1例如下.
出处 《临床皮肤科杂志》 CAS CSCD 北大核心 2004年第9期561-561,共1页 Journal of Clinical Dermatology
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参考文献2

  • 1Lindor NM, Devries EM, Michels VV, et al. Rothmund-Thomson syndrome in siblings: evidence for acquired in vivo mosaicism[J].Clin Genet, 1996, 49(3): 124-129.
  • 2Cumin I, Cohen JY, David A, et al. Rothmound-Thomson syndrome and ostesosarcoma[J]. Med Pediatr Oncol, 1996, 26(6):414-416.

同被引文献9

  • 1Macris MA, Krejci L, Bussen W, et al. Biochemical characterization of the RECQ4 protein, mutated in Rothmund-Thomson syndrome[J]. DNA Repair (Amst), 2006, 5(2): 172-180.
  • 2Lindor NM, Devries EM, Michels VV, et al. Rothmund-Thomson syndrome in siblings: evidence for acquired in vivo mosaicism[J]. Clin Genet, 1996, 49(3): 124-129.
  • 3Wang LL, Gannavarapu A, Kozinetz CA, et al. Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome [J]. J Natl Cancer Inst, 2003, 95(9): 669-674.
  • 4Durand F, Castorina P, Morant C, et al. Rothmund-Thomson syndrome, trisomy 8 mosaicism and RECQ4 gene mutation[J]. Ann Dermatol Venereol, 2002, 129(6-7): 892-895.
  • 5Kitao S, Shimamoto A, Goto M, et al. Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome[J]. Nat Genet, 1999, 22(1): 82-84.
  • 6Wang LL, Levy ML, Lewis RA, et al. Clinical manifestations in a cohort of 41 Rothmund-Thomson syndrome patients [J]. Am J Med Genet, 2001, 102(1): 11-17.
  • 7Hafidh MA, Sheahan P, Russell JD. Multiple airway abnormalities in a patient with Rothmund-Thomson syndrome [J]. Int J Pediatr Otorhinolaryngol, 2004, 68(4): 469-472.
  • 8党林,栗玉珍,于淞.Rothmund—Thomson综合征一例RECQL4基因的突变分析[J].中华皮肤科杂志,2009,42(1):28-30. 被引量:4
  • 9常建民.有皮肤异色症表现的皮肤病[J].临床皮肤科杂志,2011,40(6):377-378. 被引量:6

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