Literature DB >> 468258

Dicentric Robertsonian translocation in man. 17 cases studied by R,C, and N banding.

M G Mattei, J F Mattei, S Ayme, F Giraud.   

Abstract

The authors studied 17 cases of Robertsonian translocation. In all cases but one C banding showed that a dicentric translocation was involved. Silver staining demonstrated the presence of an NOR between the two centromeres in only one case.

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Year:  1979        PMID： 468258     DOI： 10.1007/bf00295586

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


  24 in total

Review 1.  The possibility of latent centromeres and a proposed nomenclature system for total chromosome and whole arm translocations.

Authors:  T C Hsu; S Pathak; T R Chen
Journal:  Cytogenet Cell Genet       Date:  1975

2.  ABSENCE OF RIBOSOMAL RNA SYNTHESIS IN THE ANUCLEOLATE MUTANT OF XENOPUS LAEVIS.

Authors:  D D BROWN; J B GURDON
Journal:  Proc Natl Acad Sci U S A       Date:  1964-01       Impact factor: 11.205

3.  The Prader-Willi syndrome with a 15/15 translocation. Case report and review of the literature.

Authors:  C J Hawkey; A Smithies
Journal:  J Med Genet       Date:  1976-04       Impact factor: 6.318

4.  Satellite association and variations in length of the nucleolar constriction of normal and variant human G chromosomes.

Authors:  E Orye
Journal:  Humangenetik       Date:  1974

5.  On the relationship between the frequency of association and the nucleolar constriction of individual acrocentric chromosomes.

Authors:  M Schmid; W Krone; W Vogel
Journal:  Humangenetik       Date:  1974

6.  Reexamination of a family with a t(13q14q) and a ring D(13) child.

Authors:  E Niebuhr
Journal:  Ann Genet       Date:  1973-09

7.  Dicentric and monocentric Robertsonian translocations in man.

Authors:  E Niebuhr
Journal:  Humangenetik       Date:  1972

8.  An improved technique for selective silver staining of nucleolar organizer regions in human chromosomes.

Authors:  S E Bloom; C Goodpasture
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

9.  15/15 translocation in Prader-Willi syndrome.

Authors:  M Fraccaro; O Zuffardi; E M Buhler; L P Jurik
Journal:  J Med Genet       Date:  1977-08       Impact factor: 6.318

10.  Identification of nucleolus organizer regions (NORs) in normal and neoplastic human cells by the silver-staining technique.

Authors:  H R Hubbell; T C Hsu
Journal:  Cytogenet Cell Genet       Date:  1977
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  15 in total

1.  Characterization of Robertsonian translocations by using fluorescence in situ hybridization.

Authors:  D J Wolff; S Schwartz
Journal:  Am J Hum Genet       Date:  1992-01       Impact factor: 11.025

2.  Chromosome analysis of spermatozoa from a male heterozygous for a 13;14 Robertsonian translocation.

Authors:  F Pellestor; B Sele; H Jalbert
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

3.  De novo 21/21 translocation Down syndrome. Studies of parental origin of the translocation and acrocentric associations in parents.

Authors:  J Nikolis; V Kekić
Journal:  Hum Genet       Date:  1986-06       Impact factor: 4.132

4.  Advantages of silver staining in seven rearrangements of acrocentric chromosomes, excluding Robertsonian translocations.

Authors:  M G Mattei; J F Mattei; I Vidal; F Giraud
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

5.  Satellite DNA sequences in the human acrocentric chromosomes: information from translocations and heteromorphisms.

Authors:  J R Gosden; S S Lawrie; C M Gosden
Journal:  Am J Hum Genet       Date:  1981-03       Impact factor: 11.025

6.  Molecular cytogenetic characterization of 17 rob(13q14q) Robertsonian translocations by FISH, narrowing the region containing the breakpoints.

Authors:  J Y Han; K H Choo; L G Shaffer
Journal:  Am J Hum Genet       Date:  1994-11       Impact factor: 11.025

7.  Familial reciprocal translocation t(9;13)(p11;p12) investigated by silver staining and in situ hybridisation.

Authors:  J M Varley; J Gosden; M Hultén
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

8.  Association of ribosomal genes in the fibrillar center of the nucleolus: a factor influencing translocation and nondisjunction in the human meiotic oocyte.

Authors:  C Mirre; M Hartung; A Stahl
Journal:  Proc Natl Acad Sci U S A       Date:  1980-10       Impact factor: 11.205

Review 9.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

10.  Structural basis for Robertsonian translocations in man: association of ribosomal genes in the nucleolar fibrillar center in meiotic spermatocytes and oocytes.

Authors:  A Stahl; J M Luciani; M Hartung; M Devictor; J L Bergé-Lefranc; M Guichaoua
Journal:  Proc Natl Acad Sci U S A       Date:  1983-10       Impact factor: 11.205
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