Literature DB >> 5097142

The 13q- deletion syndrome.

E Grace, J Drennan, D Colver, R R Gordon.   

Abstract

Mesh：

Year:  1971        PMID： 5097142      PMCID： PMC1469176          DOI： 10.1136/jmg.8.3.351

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  17 in total

1.  The Production of Homozygous Deficient Tissues with Mutant Characteristics by Means of the Aberrant Mitotic Behavior of Ring-Shaped Chromosomes.

Authors:  B McClintock
Journal:  Genetics       Date:  1938-07       Impact factor: 4.562

2.  Ring D1 chromosome and multiple malformations.

Authors:  M Tolksdorf; H R Wiedmann; U Goll
Journal:  Lancet       Date:  1969-11-08       Impact factor: 79.321

3.  [A case of D ring chromosome].

Authors:  N Ayraud; G Szepetowski
Journal:  Ann Genet       Date:  1969-12

4.  Multiple congenital anomalies associated with a ring-D chromosome.

Authors:  R C Juberg; M S Adams; W J Venema; M G Hart
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

5.  Chromosome abnormalities in two cases with bilateral radial element defects.

Authors:  M Faed; A Stewart; A J Keay
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

6.  Retinoblastoma and deletion D (14) syndrome.

Authors:  M G Wilson; J Melnyk; J W Towner
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

7.  Absent thumbs with a ring D2 chromosome: a new deletion syndrome.

Authors:  R S Sparkes; R E Carrel; S W Wright
Journal:  Am J Hum Genet       Date:  1967-09       Impact factor: 11.025

8.  A ring D chromosome and anomalous inheritance of haptoglobin type.

Authors:  P S Gerald; S Warner; J D Singer; P A Corcoran; I Umansky
Journal:  J Pediatr       Date:  1967-02       Impact factor: 4.406

9.  The identification of the chromosomes of the D group (13-15) Denver: an autoradiographic and measurement study.

Authors:  F Giannelli; R M Howlett
Journal:  Cytogenetics       Date:  1966

10.  Ring D chromosome: a second case associated with anomalous haptoglobin inheritance.

Authors:  G E Bloom; P S Gerald; L E Reisman
Journal:  Science       Date:  1967-06-30       Impact factor: 47.728
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  19 in total

1.  Deletion of long arms of chromosome 13.

Authors:  M Kucerovă; Z Polívková; M Pokorná
Journal:  Humangenetik       Date:  1975

Review 2.  Genetics of neoplasia--impact of ecogenetics on oncogenesis. A review.

Authors:  D T Purtilo; L Paquin; T Gindhart
Journal:  Am J Pathol       Date:  1978-06       Impact factor: 4.307

3.  D13 ring chromosome syndrome.

Authors:  A Mccandless; S Walker
Journal:  Arch Dis Child       Date:  1976-06       Impact factor: 3.791

4.  Chromosomal analysis of metastatic retinoblastoma cells.

Authors:  S Inoue; Y Ravindranath; M J Ottenbreit; R I Thompson; W W Zuelzer
Journal:  Humangenetik       Date:  1974

5.  Chromosome banding patterns in an infant with 13q minus syndrome.

Authors:  T Ikeuchi; S Sonta; M Sasaki; M Hujita; K Tsunematsu
Journal:  Humangenetik       Date:  1974-03-28

6.  Retinoblastoma and D-chromosome deletions.

Authors:  M G Wilson; J W Towner; A Fujimoto
Journal:  Am J Hum Genet       Date:  1973-01       Impact factor: 11.025

7.  Chromosome studies in twelve patients with retinoblastoma.

Authors:  A Czeizel; L Csósz; J Gárdonyi; L Remenár; P Ruziscka
Journal:  Humangenetik       Date:  1974-05-17

8.  [Anusual chromosome set (46,XX,Dq-) in osteomyelofibrosis].

Authors:  E Ganner-Millonig
Journal:  Blut       Date:  1974-06

9.  The aetiology of the cat eye syndrome reconsidered.

Authors:  G Guanti
Journal:  J Med Genet       Date:  1981-04       Impact factor: 6.318

Review 10.  Constitutional ring chromosomes and tumour suppressor genes.

Authors:  N Tommerup; R Lothe
Journal:  J Med Genet       Date:  1992-12       Impact factor: 6.318
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