Literature DB >> 7386455

Familial retinoblastoma: segregation of chromosome 13 in four families.

L A Knight, H A Gardner, B L Gallie.   

Abstract

Fluorescent markers on chromosome 13 have been used to study familial retinoblastoma. One family showed concordant segregation of a particular chromosome 13 and retinoblastoma from the affected parent to the affected children. In three other families, segregation was discordant. Meiotic crossing over with recombination is proposed as the explanation.

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Mesh：

Year:  1980        PMID： 7386455      PMCID： PMC1685996     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


  9 in total

1.  CHROMOSOME DELETION IN A CASE OF RETINOBLASTOMA.

Authors:  K P LELE; L S PENROSE; H B STALLARD
Journal:  Ann Hum Genet       Date:  1963-11       Impact factor: 1.670

2.  Chromosomal deletion and retinoblastoma.

Authors:  A G Knudson; A T Meadows; W W Nichols; R Hill
Journal:  N Engl J Med       Date:  1976-11-11       Impact factor: 91.245

3.  The practical management of retinoblastoma.

Authors:  R M Ellsworth
Journal:  Trans Am Ophthalmol Soc       Date:  1969

4.  Spontaneous resolution of probable retinoblastoma.

Authors:  R J Brockhurst; D D Donaldson
Journal:  Arch Ophthalmol       Date:  1970-09

5.  Segregation of chromosome 13 in retinoblastoma.

Authors:  L A Knight; H A Gardner; B L Gallie
Journal:  Lancet       Date:  1978-05-06       Impact factor: 79.321

6.  The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability.

Authors:  T Caspersson; G Lomakka; L Zech
Journal:  Hereditas       Date:  1972       Impact factor: 3.271

7.  Retinoblastoma and subband deletion of chromosome 13.

Authors:  J J Yunis; N Ramsay
Journal:  Am J Dis Child       Date:  1978-02

8.  Retinoblastoma with 13q- chromosomal deletion associated with maternal paracentric inversion of 13q.

Authors:  R S Sparkes; H Muller; I Klisak
Journal:  Science       Date:  1979-03-09       Impact factor: 47.728

9.  Chromosome analysis on 930 consecutive newborn children using quinacrine fluorescent banding technique.

Authors:  C C Lin; M M Gedeon; P Griffith; W K Smink; D R Newton; L Wilkie; L M Sewell
Journal:  Hum Genet       Date:  1976-03-12       Impact factor: 4.132
  9 in total
  6 in total

Review 1.  Putative non-Mendelian transmission of retinoblastoma in males: a phenotypic segregation analysis of 150 pedigrees.

Authors:  F L Munier; L Arabien; P Flodman; M A Spence; G Pescia; H P Rutz; A L Murphree
Journal:  Hum Genet       Date:  1994-11       Impact factor: 4.132

2.  Crossing-over during human spermatogenesis visualized cytologically.

Authors:  I Hansmann; M Geisler; T Grimm
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

3.  Chiasma derived genetic maps and recombination fractions: chromosome 13 with reference to the proposed 13q14 retinoblastoma locus.

Authors:  R W Palmer; M A Hultén
Journal:  J Med Genet       Date:  1982-04       Impact factor: 6.318

4.  Family studies on the chromosomal location of the retinoblastoma gene (Rb-1).

Authors:  J Morten; D G Harnden; S Bundey
Journal:  J Med Genet       Date:  1982-04       Impact factor: 6.318

5.  Location of the retinoblastoma susceptibility gene(s) and the human esterase D locus.

Authors:  P Ward; S Packman; W Loughman; M Sparkes; R Sparkes; A McMahon; T Gregory; A Ablin
Journal:  J Med Genet       Date:  1984-04       Impact factor: 6.318

6.  Hereditary retinoblastoma: lack of maternal effect.

Authors:  E Matsunaga
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132
  6 in total

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