메뉴 건너뛰기




Volumn 27, Issue 9, 2007, Pages 874-878

Prenatal diagnosis and prenatal imaging features of fetal monosomy 1p36

Author keywords

1p36 deletion; Monosomy 1p36; Prenatal diagnosis

Indexed keywords

ALPHA FETOPROTEIN;

EID: 34548751136     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1796     Document Type: Article
Times cited : (13)

References (19)
  • 1
    • 0042232610 scopus 로고    scopus 로고
    • Monosomy 1p36 breakpoint junctions suggest pre-meitotic breakage-fusion-bridge cycles are involved in generating terminal deletions
    • Baliff B, Yu W, Shaw C, Kashork C, Shaffer L. 2003. Monosomy 1p36 breakpoint junctions suggest pre-meitotic breakage-fusion-bridge cycles are involved in generating terminal deletions. Hum Mol Genet 12: 21533-22165.
    • (2003) Hum Mol Genet , vol.12 , pp. 21533-22165
    • Baliff, B.1    Yu, W.2    Shaw, C.3    Kashork, C.4    Shaffer, L.5
  • 2
    • 0035152035 scopus 로고    scopus 로고
    • Tumour suppressor genes on the short arm of chromosome 1 in neuroblastoma
    • Blatt J. 2001. Tumour suppressor genes on the short arm of chromosome 1 in neuroblastoma. Pediatr Hematol Oncol 18: 3-5.
    • (2001) Pediatr Hematol Oncol , vol.18 , pp. 3-5
    • Blatt, J.1
  • 3
    • 0033048717 scopus 로고    scopus 로고
    • A case of recurrent congenital fetal anomalies associated with a familial subtelomeric translocation
    • Brackley KJ, Kilby MD, Morton J, Whittle MJ, Knight SJ, Flint J. 1999. A case of recurrent congenital fetal anomalies associated with a familial subtelomeric translocation. Prenat Diagn 19(6): 570-574.
    • (1999) Prenat Diagn , vol.19 , Issue.6 , pp. 570-574
    • Brackley, K.J.1    Kilby, M.D.2    Morton, J.3    Whittle, M.J.4    Knight, S.J.5    Flint, J.6
  • 4
    • 0036334452 scopus 로고    scopus 로고
    • Loss of the SKI protooncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski_/_mice
    • Colmenares C, Heilstedt HA, Shaffer LG, et al. 2002. Loss of the SKI protooncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski_/_mice. Nat Genet 30: 106-109.
    • (2002) Nat Genet , vol.30 , pp. 106-109
    • Colmenares, C.1    Heilstedt, H.A.2    Shaffer, L.G.3
  • 5
    • 0032899034 scopus 로고    scopus 로고
    • Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature
    • Faivre L, Morichoon-Delvallez N, Viot G, et al. 1999. Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature. Prenat Diagn 19: 45-49.
    • (1999) Prenat Diagn , vol.19 , pp. 45-49
    • Faivre, L.1    Morichoon-Delvallez, N.2    Viot, G.3
  • 6
    • 0035101844 scopus 로고    scopus 로고
    • Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation
    • Giraudeau F, Taine L, Biancalana V, et al. 2001. Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation. J Med Genet 38: 121-125.
    • (2001) J Med Genet , vol.38 , pp. 121-125
    • Giraudeau, F.1    Taine, L.2    Biancalana, V.3
  • 7
    • 0141955800 scopus 로고    scopus 로고
    • Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality
    • Heilstedt HA, Ballif BA, Howard LA, Kashork CD, Shaffer LG. 2003a. Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality. Clin Genet 64: 310-316.
    • (2003) Clin Genet , vol.64 , pp. 310-316
    • Heilstedt, H.A.1    Ballif, B.A.2    Howard, L.A.3    Kashork, C.D.4    Shaffer, L.G.5
  • 8
    • 0038406165 scopus 로고    scopus 로고
    • Physical map of 1p36, placement of breakpoints in monosomy 1p36 and clinical characterisation of the syndrome
    • Heilstedt HA, Ballif BC, Howard LA, et al. 2003b. Physical map of 1p36, placement of breakpoints in monosomy 1p36 and clinical characterisation of the syndrome. Am J Hum Genet 72: 1200-1212.
    • (2003) Am J Hum Genet , vol.72 , pp. 1200-1212
    • Heilstedt, H.A.1    Ballif, B.C.2    Howard, L.A.3
  • 9
    • 0034785511 scopus 로고    scopus 로고
    • Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome
    • Heilstedt HA, Burgess DL, Anderson AE, et al. 2001. Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome. Epilepsia 42: 1103-1111.
    • (2001) Epilepsia , vol.42 , pp. 1103-1111
    • Heilstedt, H.A.1    Burgess, D.L.2    Anderson, A.E.3
  • 10
    • 0030812331 scopus 로고    scopus 로고
    • Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers
    • Kaghad M, Bonnet H, Yang A, et al. 1997. Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers. Cell 90(4): 809-819.
    • (1997) Cell , vol.90 , Issue.4 , pp. 809-819
    • Kaghad, M.1    Bonnet, H.2    Yang, A.3
  • 11
    • 0034667246 scopus 로고    scopus 로고
    • Chromosome abnormalities in malignant melanoma: Clinical significance of non random chromosome abnormalities in 206 cases
    • Nelson MA, Radmacher MD, Simon R, et al. 2000. Chromosome abnormalities in malignant melanoma: clinical significance of non random chromosome abnormalities in 206 cases. Cancer Genet Cytogenet 122: 101-109.
    • (2000) Cancer Genet Cytogenet , vol.122 , pp. 101-109
    • Nelson, M.A.1    Radmacher, M.D.2    Simon, R.3
  • 12
    • 29644436953 scopus 로고    scopus 로고
    • p73, a sophisticated p53 family member in the cancer world
    • Ozaki T, Nakagawara A. 2005. p73, a sophisticated p53 family member in the cancer world. Cancer Sci 96(11): 729-737.
    • (2005) Cancer Sci , vol.96 , Issue.11 , pp. 729-737
    • Ozaki, T.1    Nakagawara, A.2
  • 13
    • 0030870848 scopus 로고    scopus 로고
    • Chromosome 1p36 deletions: The clinical phenotype and molecular characterisation of a common newly delineated syndrome
    • Shapira SK, McCaskill C, Northrup H, et al. 1997. Chromosome 1p36 deletions: The clinical phenotype and molecular characterisation of a common newly delineated syndrome. Am J Hum Genet 61: 642-650.
    • (1997) Am J Hum Genet , vol.61 , pp. 642-650
    • Shapira, S.K.1    McCaskill, C.2    Northrup, H.3
  • 14
    • 0036362854 scopus 로고    scopus 로고
    • Molecular characterization of 18p deletions: Evidence for a breakpoint cluster
    • Schaub RL, Reveles XT, Baillargeon J, Leach RJ, Cody JD. 2002. Molecular characterization of 18p deletions: evidence for a breakpoint cluster. Genet Med 4: 15-19.
    • (2002) Genet Med , vol.4 , pp. 15-19
    • Schaub, R.L.1    Reveles, X.T.2    Baillargeon, J.3    Leach, R.J.4    Cody, J.D.5
  • 16
    • 0030741911 scopus 로고    scopus 로고
    • Band 1p36 abnormalities and t(1;17) in ovarian carcinoma
    • Thompson FH, Taetle R, Trent JM, et al. 1997. Band 1p36 abnormalities and t(1;17) in ovarian carcinoma. Cancer Genet Cytogenet 96: 106-110.
    • (1997) Cancer Genet Cytogenet , vol.96 , pp. 106-110
    • Thompson, F.H.1    Taetle, R.2    Trent, J.M.3
  • 18
    • 0032898935 scopus 로고    scopus 로고
    • Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletions
    • Wu Y-Q, Heilstedt H, Bedell JA, et al. 1999. Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletions. Hum Mol Genet 8: 313-321.
    • (1999) Hum Mol Genet , vol.8 , pp. 313-321
    • Wu, Y.-Q.1    Heilstedt, H.2    Bedell, J.A.3
  • 19
    • 10744221541 scopus 로고    scopus 로고
    • Development of a comparative genomic hybridisation microarray and demonstration of its utility with 25 well characterized 1p36 deletions
    • Yu W, Ballif B, Kashork C, et al. 2003. Development of a comparative genomic hybridisation microarray and demonstration of its utility with 25 well characterized 1p36 deletions. Hum Mol Genet 12: 2145-2152.
    • (2003) Hum Mol Genet , vol.12 , pp. 2145-2152
    • Yu, W.1    Ballif, B.2    Kashork, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.