Interstitial deletion of chromosome 13 involving the region 13q14.

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Hum Genet. 1987 Nov;77(3):292-3. doi: 10.1007/BF00284490.

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A chromosomal breakpoint that separates the esterase D and retinoblastoma predisposition loci in a patient with del(13)(q14q31).

Cancer Genet Cytogenet. 1987 Jul;27(1):27-31. doi: 10.1016/0165-4608(87)90256-1.

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Deletion (13)(q13q14.3) with retinoblastoma: confirmation and extension of a recognisable pattern of clinical features in retinoblastoma patients with 13q deletion.

J Med Genet. 1987 Nov;24(11):696-7. doi: 10.1136/jmg.24.11.696.

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Familial retinoblastoma (mother and son) with 13q14 deletion.

Hum Genet. 1987 Oct;77(2):104-7. doi: 10.1007/BF00272373.

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Molecular evidence that the esterase-D gene lies proximal to the retinoblastoma susceptibility locus in chromosome region 13q14.

Hum Genet. 1988 Dec;81(1):57-60. doi: 10.1007/BF00283730.

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De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastoma.

Hum Genet. 1987 Sep;77(1):51-4. doi: 10.1007/BF00284713.

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The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletions.

Arch Dis Child. 1987 Jan;62(1):8-11. doi: 10.1136/adc.62.1.8.

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Incidence and significance of a deletion of chromosome band 13q14 in patients with retinoblastoma and in their families.

Ophthalmology. 1984 Dec;91(12):1695-9. doi: 10.1016/s0161-6420(84)34090-8.

9

Types, rates, origin and expressivity of chromosome mutations involving 13q14 in retinoblastoma patients.

Hum Genet. 1988 Jun;79(2):118-23. doi: 10.1007/BF00280548.

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Deletion of chromosome region 13q14 is transmissible and does not always predispose to retinoblastoma.

Hum Genet. 1988 Sep;80(1):43-5. doi: 10.1007/BF00451453.

引用本文的文献

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Molecular detection of chromosomal translocations that disrupt the putative retinoblastoma susceptibility locus.

Mol Cell Biol. 1989 Jan;9(1):1-5. doi: 10.1128/mcb.9.1.1-5.1989.

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Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase D.

Science. 1983 Feb 25;219(4587):971-3. doi: 10.1126/science.6823558.

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Separation of retinoblastoma and esterase D loci in a patient with sporadic retinoblastoma and del(13)(q14.1q22.3).

Hum Genet. 1984;68(3):258-9. doi: 10.1007/BF00418397.

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Patient with 13 chromosome deletion: evidence that the retinoblastoma gene is a recessive cancer gene.

Science. 1983 Feb 25;219(4587):973-5. doi: 10.1126/science.6336308.

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Mutation and cancer: statistical study of retinoblastoma.

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Genetic origin of mutations predisposing to retinoblastoma.

Science. 1985 Apr 26;228(4698):501-3. doi: 10.1126/science.3983638.

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Evidence for a null allele at the esterase D (EC 3.1.1.1) locus.

Hum Genet. 1979 Feb 15;46(3):319-23. doi: 10.1007/BF00273315.

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