Literature DB >> 5345106

Retinoblastoma and deletion D (14) syndrome.

M G Wilson, J Melnyk, J W Towner.   

Abstract

Entities:  

Mesh：

Year:  1969        PMID： 5345106      PMCID： PMC1468747          DOI： 10.1136/jmg.6.3.322

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


× No keyword cloud information.
  16 in total

1.  Chromosome studies in retinoblastoma.

Authors:  S WIENER; A B REESE; G A HYMAN
Journal:  Arch Ophthalmol       Date:  1963-03

2.  Ring chromosomes in human beings.

Authors:  H C WANG; J MELNYK; L T McDONALD; I A UCHIDA; D H CARR; B GOLDBERG
Journal:  Nature       Date:  1962-08-18       Impact factor: 49.962

3.  Multiple congenital abnormalities associated with ring chromosome.

Authors:  A D BAIN; I K GAULD
Journal:  Lancet       Date:  1963-08-10       Impact factor: 79.321

4.  Quantitative genetics of finger-print patterns.

Authors:  S B HOLT
Journal:  Br Med Bull       Date:  1961-09       Impact factor: 4.291

5.  [Deletion of the short arm of a 13-15 chromosome, hypertelorism and Hp0 haptoglobin phenotype in the same family].

Authors:  J de Grouchy; C Salmon; D Salmon; P Maroteaux
Journal:  Ann Genet       Date:  1966-06

6.  Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome.

Authors:  A I Taylor
Journal:  J Med Genet       Date:  1968-09       Impact factor: 6.318

7.  Haptoglobin: a locus on the D1 chromosome?

Authors:  W B Bias; B R Migeon
Journal:  Am J Hum Genet       Date:  1967-05       Impact factor: 11.025

8.  A human ring D chromosome associated with multiple congenital abnormalities.

Authors:  R L Teplitz; D Miller; K M Hansson; T S Rundall
Journal:  J Pediatr       Date:  1967-06       Impact factor: 4.406

9.  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

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
View more
  23 in total

1.  Deletion long arm 13.

Authors:  J Nielsen; A Homma; F Christiansen; K Rasmussen; P Saldaña-Garcia
Journal:  Hum Genet       Date:  1977-07-26       Impact factor: 4.132

Review 2.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

Authors:  G Töndury
Journal:  Humangenetik       Date:  1973-03-23

3.  Chromosomal analysis of metastatic retinoblastoma cells.

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

4.  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

5.  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

Review 6.  Growing points in cell pathology. Cytogenetic aspects.

Authors:  P E Polani
Journal:  Proc R Soc Med       Date:  1970-09

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

Review 9.  Population cytogenetics, assignment of gene loci in autosomes, karyotype-phenotype correlations. A progress report on human cytogenetics.

Authors:  E Passarge
Journal:  Humangenetik       Date:  1970

10.  A prisoner with an unusual karyotype (46,XY,Dq-).

Authors:  J Kahn; F Reed
Journal:  J Med Genet       Date:  1971-09       Impact factor: 6.318
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.