Literature DB >> 6502652

A familial insertion involving an active nucleolar organiser within chromosome 12.

J L Watt, D A Couzin, D J Lloyd, G S Stephen, E McKay.   

Abstract

As far as the authors are aware this is the first report of the insertion of an active NOR into a non-acrocentric chromosome, although a simple translocation involving an active NOR has been previously recorded. More specifically, this case involves the non-reciprocal translocation of the centromere and stalk of an acrocentric into 12p, generating an apparently stable dicentric chromosome. The insertion is seen in three generations and may be relatively genetically benign. The abnormality is fully described by G and sequential C banding, DA/DAPI fluorescence, kinetochore staining, and Ag-NOR staining, and the findings are discussed in the light of the limited published reports of insertion in man.

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Year:  1984        PMID: 6502652      PMCID: PMC1049324          DOI: 10.1136/jmg.21.5.379

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


  22 in total

1.  "Cri du chat" syndrome with maternal insertional translocation.

Authors:  R Berger; G Touati; J Derre; M A Ortiz; J Martinetti
Journal:  Clin Genet       Date:  1974       Impact factor: 4.438

2.  Complex five-break rearrangement.

Authors:  M G Fitzgerald
Journal:  Clin Genet       Date:  1974-01       Impact factor: 4.438

3.  Familial insertional translocation.

Authors:  E Grace; G R Sutherland; A D Bain
Journal:  Lancet       Date:  1972-07-29       Impact factor: 79.321

4.  An interstitial translocation: chromosome no. 1p to 4q.

Authors:  J E Gray; J E Syrett; K M Ritchie; W D Elliott
Journal:  Lancet       Date:  1972-07-08       Impact factor: 79.321

5.  Interstitial translocation in man.

Authors:  L R Shapiro; D Warburton
Journal:  Lancet       Date:  1972-09-30       Impact factor: 79.321

6.  A cytogenetic survey of 11,680 newborn infants.

Authors:  P A Jacobs; M Melville; S Ratcliffe; A J Keay; J Syme
Journal:  Ann Hum Genet       Date:  1974-05       Impact factor: 1.670

7.  [Trisomy for the distal part of the short arm of the number 3 chromosome in 3 siblings. First example of chromosomal insertion: INS(7;3)(q 31;p 21 p 26)].

Authors:  M O Rethoré; J Lejeune; S Carpentier; M Prieur; B Dutrillaux; P Seringe; A Rossier; J C Job
Journal:  Ann Genet       Date:  1972-09

8.  Presumptive direct insertion within chromosome 2 in man.

Authors:  A J Therkelsen; M Hultén; J Jonasson; J Lindsten; N C Christensen; T Iversen
Journal:  Ann Hum Genet       Date:  1973-04       Impact factor: 1.670

9.  Familial mental retardation in a family with an inherited chromosome rearrangement.

Authors:  A E Chudley; F Bauder; M Ray; P J McAlpine; S D Pena; J L Hamerton
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

10.  Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21.

Authors:  J D Williams; R L Summitt; P R Martens; R A Kimbrell
Journal:  Am J Hum Genet       Date:  1975-07       Impact factor: 11.025

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  5 in total

1.  A molecular deletion of distal chromosome 4p in two families with a satellited chromosome 4 lacking the Wolf-Hirschhorn syndrome phenotype.

Authors:  L L Estabrooks; A N Lamb; H N Kirkman; N P Callanan; K W Rao
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

2.  A new multicolor fluorescence in situ hybridization probe set directed against human heterochromatin: HCM-FISH.

Authors:  Maria Bucksch; Monika Ziegler; Nadezda Kosayakova; Milene V Mulatinho; Milene V Mulhatino; Juan C Llerena; Susanne Morlot; Wolfgang Fischer; Anna D Polityko; Anna I Kulpanovich; Michael B Petersen; Britta Belitz; Vladimir Trifonov; Anja Weise; Thomas Liehr; Ahmed B Hamid
Journal:  J Histochem Cytochem       Date:  2012-04-17       Impact factor: 2.479

3.  A non-centromeric C band variant on chromosome 11q23.2.

Authors:  D K Spak; K Johnston; T A Donlon
Journal:  J Med Genet       Date:  1989-08       Impact factor: 6.318

4.  A de novo satellited short arm of the Y chromosome possibly resulting from an unstable translocation.

Authors:  C L Lin; L Gibson; B Pober; T L Yang-Feng
Journal:  Hum Genet       Date:  1995-11       Impact factor: 4.132

5.  Outcome after prenatal detection of a sporadic, unstable translocation t(5;21).

Authors:  A O Martin; I Benuck; H S Traisman; M S Swanson; N Trakas; K Laing; B J Rosinsky; J Beaird; E S Traisman; S Elias
Journal:  J Med Genet       Date:  1986-06       Impact factor: 6.318

  5 in total

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