Citations for
1DEL13Q14
Genotype-phenotype correlations in patients with retinoblastoma and interstitial 13q deletions.
Mitter D, Ullmann R, Muradyan A, Klein-Hitpaß L, Kanber D, Ounap K, Kaulisch M, Lohmann D.
Eur J Hum Genet 19(9):947-958. doi: 10.1038/ejhg.2011.58. Epub 2011 Apr 20. 2011
2DEL13Q14, RB, RB1
Genotype-phenotype correlations in patients with retinoblastoma and interstitial 13q deletions.
Mitter D, Ullmann R, Muradyan A, Klein-Hitpass L, Kanber D, Ounap K, Kaulisch M, Lohmann D.
Eur J Hum Genet 19(9):947-58. doi: 10.1038/ejhg.2011.58. Epub 2011 Apr 20. 2011
3DEL13q14
Interstitial deletion of 13q associated with polymicrogyria.
Kogan JM, Egelhoff JC, Saal HM.
Am J Med Genet A [Epub ahead of print] 2008
4RB, DEL13Q14, RB1
Retinoblastoma: revisiting the model prototype of inherited cancer.
Lohmann DR, Gallie BL.
Am J Med Genet C Semin Med Genet 129(1):23-8. Review. 2004
5DEL13Q14,RB
Retinoblastoma in a patient with an X;13 translocation and facial abnormalities consistent with 13q-syndrome.
Laquis SJ, Rodriguez-Galindo C, Wilson MW, Fleming JC, Haik BG.
Am J Ophthalmol 133(2):285-7. 2002
6DEL13Q14,RB,RB1
Dysmorphic phenotype and neurological impairment in 22 retinoblastoma patients with constitutional cytogenetic 13q deletion.
Baud O, et al.
Clin Genet 55(6):478-82. 1999
7DEL13Q14,RB
Bilateral retinoblastoma in a male patient with an X; 13 translocation: evidence for silencing of the RB1 gene by the spreading of X inactivation.
Jones C, Booth C, Rita D, Jazmines L, Brandt B, Newlan A, Horsthemke B.
Am J Hum Genet 60(6):1558-62. No abstract available. 1997
8DEL13Q14,RB,RB1
Cytogenetic and molecular investigation of a balanced Xq13q translocation in a patient with retinoblastoma.
Stambolian D, et al.
Am J Med Genet 42 : 771-776. 1992
9DEL13Q14,RB,RB1
Molecular detection of constitutional deletions in patients with retinoblastoma.
Blanquet V, Creau-Goldberg N, de Grouchy J, Turleau C.
Am J Med Genet 39(3):355-61. 1991
10DEL13Q14,RB,RB1
Constitutional deletions predisposing to retinoblastoma.
Janson M, et al.
Hum Genet 85 : 21-24. 1990
11DEL13Q14,RB,RB1
Deletion of chromosome region 13q14 is transmissible and does not always predispose to retinoblastoma.
Cowell JK, et al.
Hum Genet 80 : 43-45. 1988
12DEL13Q14,RB,RB1
Molecular detection and differentiation of deletions in band 13q14 in human retinoblastoma.
Lalande M, et al.
Cancer Genet Cytogenet 23 : 151-157. 1986
13DEL13Q14,RB,RB1
Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas.
Dryja TP, et al.
Proc Natl Acad Sci U S A 83 : 7391-7394. 1986
14DEL13Q14
Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition.
Hansen MF, et al.
Proc Natl Acad Sci U S A 82 : 6216-6220. 1985
15DEL13Q14,RB,RB1
Cytogenetic forms of retinoblastoma : their incidence in a survey of 66 patients.
Turleau C, et al.
Cancer Genet Cytogenet 16 : 321-334. 1985
16DEL13Q14,RB,RB1
Retinoblastoma in a boy with a de novo mutation of a 13/18 translocation: The assumption that the retinoblastoma locus is at 13q141, particularly at the distal portion of it.
Motegi T, et al.
Hum Genet 60 : 193-195. 1982
17DEL13Q14, RB, RB1
Familial retinoblastoma and chromosome 13 deletion transmitted via insertional translocation.
Strong LC, et al.
Science 213 : 1501-1503. 1981
18DEL13Q14,RB
Retinoblastoma-del(13q14): report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase D.
Rivera H, Turleau C, de Grouchy J, Junien C, Despoisse S, Zucker JM.
Hum Genet 59(3):211-4. 1981
19DUP13Q, DEL13QD, DEL13Q14, DEL13Q32
Partial deletions and trisomies of chromosome 13; mapping of bands associated with particular malformations.
Noel B, Quack B, Rethore MO.
Clin Genet 9(6):593-602. 1976
20DEL13Q14, RB, RB1
Chromosome deletion in a case of retinoblastoma.
Lele KP, et al.
Ann Hum Genet 27 : 171-174. 1963