Literature DB >> 6604013

A new familial "fragile site" on chromosome 16 (q23-24). Cytogenetic and clinical considerations.

F Shabtai, D Klar, R Nissimov, D Vardimon, J Hart, I Halbrecht.   

Abstract

A new familial fragile site at 16q23-24 is documented, and the clinical and cytogenetic data on three families and some individual patients are reported. The importance of differentiating this fragile site from that recognized previously at 16q22 is pointed out.

Entities:  

Mesh：

Year:  1983        PMID： 6604013     DOI： 10.1007/bf00279409

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  6 in total

1.  Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture.

Authors:  G R Sutherland
Journal:  Am J Hum Genet       Date:  1979-03       Impact factor: 11.025

2.  Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics.

Authors:  G R Sutherland
Journal:  Am J Hum Genet       Date:  1979-03       Impact factor: 11.025

3.  Heritable fragile sites on human chromosomes. VI. Characterization of the fragile site at 12q13.

Authors:  G R Sutherland; L Hinton
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

4.  Familial fragility on chromosome 16 (fra 16q22) enhanced by both interferon and Distamycin A.

Authors:  F Shabtai; D Klar; S Bichacho; J Hart; I Halbrecht
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

5.  Heritable fragile sites and lymphocyte culture medium containing BrdU.

Authors:  J M Scheres; T W Hustinx
Journal:  Am J Hum Genet       Date:  1980-07       Impact factor: 11.025

6.  Chromosome 17 has a real fragile site at p12.

Authors:  F Shabtai; D Klar; I Halbrecht
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132
  6 in total
  9 in total

1.  Fragile sites induced by FUdR, caffeine, and aphidicolin. Their frequency, distribution, and analysis.

Authors:  P N Rao; N A Heerema; C G Palmer
Journal:  Hum Genet       Date:  1988-01       Impact factor: 4.132

2.  A heritable fragile 12q24.13 segregating in a family with the fragile X chromosome.

Authors:  A P Amarose; P R Huttenlocher; R M Sprudzs; T J Laitsch; M J Pettenati
Journal:  Hum Genet       Date:  1987-01       Impact factor: 4.132

3.  Nonrandom distribution of methotrexate-induced aberrations on human chromosomes. Detection of further folic acid sensitive fragile sites.

Authors:  G Barbi; P Steinbach; W Vogel
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

4.  Human chromosome hot points. 1. Hot point at 3p14 in three populations.

Authors:  X T Zhou; B H Xu; C L Chu; G F Xia; N Li; R Sha
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

5.  The effect of 1-beta-D-arabinofuranosyl-cytosine on the expression of the common fragile site at 3p14.

Authors:  X Z Li; Z A Yan; X T Zhou
Journal:  Hum Genet       Date:  1986-12       Impact factor: 4.132

6.  Fragile sites and structural rearrangements in cancer.

Authors:  M De Braekeleer; B Smith; C C Lin
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

7.  DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes.

Authors:  T W Glover; C Berger; J Coyle; B Echo
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  Homozygosity for fragile site at 17p12 in a 28-year-old healthy man.

Authors:  V Izakovic
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  Human chromosome hot points. IV. Uridine-induced hot-point breaks at 3p14 and 16q23-24 and increased expression of fragile site Xq27 in folate-free medium.

Authors:  N Li; X T Zhou
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.