Literature DB >> 6174409

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

J M Varley, J Gosden, M Hultén.   

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Year:  1981        PMID： 6174409     DOI： 10.1007/BF00295484

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


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  46 in total

1.  New technique for distinguishing between human chromosomes.

Authors:  A T Sumner; H J Evans; R A Buckland
Journal:  Nat New Biol       Date:  1971-07-07

2.  Pericentric inversion of chromosome 9.

Authors:  D E Mutton; M G Daker
Journal:  Nat New Biol       Date:  1973-01-17

3.  The localization of rDNA in small, nucleolus-like structures in human diplotene oocyte nuclei.

Authors:  D J Wolgemuth-Jarashow; G M Jagiello; A S Henderson
Journal:  Hum Genet       Date:  1977-04-07       Impact factor: 4.132

4.  Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18.

Authors:  R L Neu; C C Ortega; G A Barg; W Pinto; L I Gardner; W M Howell; T E Denton
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

5.  Differential staining of the satellite regions of human acrocentric chromosomes.

Authors:  W M Howell; T E Denton; J R Diamond
Journal:  Experientia       Date:  1975-02-15

6.  Polymorphism of chromosome 9 in 600 Greek subjects.

Authors:  C Metaxotou; A Kalpini-Mavrou; M Panagou; C Tsenghi
Journal:  Am J Hum Genet       Date:  1978-01       Impact factor: 11.025

7.  t(9/22) with centric fission and NOR translocation leading to a case of pure 9p trisomy in the offspring.

Authors:  N Archidiacono; M Rocchi; U de Vonderweid; G Filippi
Journal:  Hum Genet       Date:  1978-02-16       Impact factor: 4.132

8.  The identification of human chromosomes by quinacrine fluorescence after hybridisation in situ.

Authors:  S S Lawrie; J R Gosden
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

9.  Patterns of silver staining of human chromosomes.

Authors:  J M Varley
Journal:  Chromosoma       Date:  1977-05-23       Impact factor: 4.316

10.  Trisomy 9p resulting from de novo 9/15 translocation and a 9p isochromosome.

Authors:  K R Sandig; J Mücke; H Veit
Journal:  Hum Genet       Date:  1979-11       Impact factor: 4.132
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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.  Inheritance of ribosomal gene activity and level of DNA methylation of individual gene clusters in a three generation family.

Authors:  A de Capoa; C Aleixandre; M P Felli; L Ravenna; M A Costantino; P Giancotti; O Vicenti; I Poggesi; C Grappelli; D A Miller
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

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

Authors:  J L Watt; D A Couzin; D J Lloyd; G S Stephen; E McKay
Journal:  J Med Genet       Date:  1984-10       Impact factor: 6.318

4.  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.  Cytogenetic and molecular analyses of de novo translocation dic(9;13)(p11.2;p12) in an infertile male.

Authors:  Ewa Wiland; Marta Olszewska; Andrew Georgiadis; Nataliya Huleyuk; Barbara Panasiuk; Danuta Zastavna; Svetlana A Yatsenko; Piotr Jedrzejczak; Alina T Midro; Alexander N Yatsenko; Maciej Kurpisz
Journal:  Mol Cytogenet       Date:  2014-02-21       Impact factor: 2.009
  5 in total

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