Literature DB >> 1184005

A 6p trisomy detected in a family with a "giant satellite".

H Chiyo, Y Kuroki, I Matsui, K Yanagida, Y Nakagome.   

Abstract

A very large (giant) satellite was observed on one of the D-group chromosomes of a malformed and mentally retarded infant and her father. Detailed cytogenetic studies revealed that the giant satellite represented, in fact, a der(15) chromosome of translocation t(6;15)(p21;p12 or 13). The proposita was trisomic for a part of 6p(6pter leads to 6p21). The father was a balanced carrier, however, the deletion of the short arm of a No. 6 was hard to detect in routine karyotype analysis.

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Year:  1975        PMID: 1184005     DOI: 10.1007/bf00273632

Source DB:  PubMed          Journal:  Humangenetik        ISSN: 0018-7348


  11 in total

1.  Letter: Brilliantly fluorescing enlarged short arms D or G.

Authors:  J Nielsen; U Friedrich; A B Hreidarsson; B Noel; B Quack; J Mottet
Journal:  Lancet       Date:  1974-05-25       Impact factor: 79.321

2.  G-group chromosomes in satellite associations.

Authors:  Y Nakagome
Journal:  Cytogenet Cell Genet       Date:  1973

3.  [Giemsa-R-banding analysis of the trisomy 9p and report of a new case].

Authors:  M O Rethoré; H Hoehn; H D Rott; J Couturier; B Dutrillaux; J Lejeune
Journal:  Humangenetik       Date:  1973-04-16

4.  A simple technique for demonstrating centromeric heterochromatin.

Authors:  A T Sumner
Journal:  Exp Cell Res       Date:  1972-11       Impact factor: 3.905

5.  A case of trisomy 9.

Authors:  M Feingold; L Atkins
Journal:  J Med Genet       Date:  1973-06       Impact factor: 6.318

6.  Trisomy 10 with mosaicism. A clinical and cytogenetic entity.

Authors:  Y Nakagome; K Iinuma; I Matsui
Journal:  Jinrui Idengaku Zasshi       Date:  1973-09

7.  Trisomy-8 syndrome.

Authors:  E Tuncbilek; C Halicioglu; B Say
Journal:  Humangenetik       Date:  1974-06-26

8.  Giant satellites or translocation?

Authors:  M G Wilson; A Fujimoto; N W Shinno; J W Towner
Journal:  Cytogenet Cell Genet       Date:  1973

9.  Human karyotype polymorphism. I. Routine and fluorescence microscopic investigation of chromosomes in a normal adult population.

Authors:  A V Mikelsaar; S J Tüür; M E Käosaar
Journal:  Humangenetik       Date:  1973

10.  Inherited pericentric inversion of a group D (13-15) chromosome.

Authors:  R B Surana; P E Conen
Journal:  J Med Genet       Date:  1972-03       Impact factor: 6.318

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  10 in total

1.  Partial trisomy 6p.

Authors:  A Bernheim; R Berger; G Vaugier; J C Thieffry; Y Matet
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

2.  Pitfalls in the use of chromosome variants for paternity dispute cases.

Authors:  Y Nakagome; T Kitagawa; K Iinuma; E Matsunaga; T Shinoda
Journal:  Hum Genet       Date:  1977-07-26       Impact factor: 4.132

3.  Partial trisomy 6p due to familial translocation t(6;20)(p21;p13). A new syndrome?

Authors:  M H Breuning; J B Bijlsma; H F de France
Journal:  Hum Genet       Date:  1977-08-31       Impact factor: 4.132

4.  Partial trisomy 6p and partial trisomy 22 resulting from 3:1 meiotic disjunction of maternal (6p;22q) translocation.

Authors:  P R Scarbrough; A J Carroll; S C Finley; K Hamerick
Journal:  J Med Genet       Date:  1986-04       Impact factor: 6.318

5.  Inversion duplication of chromosome 6 with trisomic codominant expression of HLA antigens.

Authors:  G Pearson; J D Mann; J Bensen; R W Bull
Journal:  Am J Hum Genet       Date:  1979-01       Impact factor: 11.025

6.  Prenatal diagnosis of a 13p+ karyotype.

Authors:  D Soudek
Journal:  Hum Genet       Date:  1979-10-02       Impact factor: 4.132

7.  The megacystis-microcolon-intestinal hypoperistalsis syndrome: a fatal autosomal recessive condition.

Authors:  D G Penman; R J Lilford
Journal:  J Med Genet       Date:  1989-01       Impact factor: 6.318

8.  Trisomy 6p22 leads to 6pter due to familial t(6;13)(p22;q34 or 33) translocation.

Authors:  G Rosi; G Venti; G Migliorini Brushelli; E Donti; V Bocchini; R Armellini
Journal:  Hum Genet       Date:  1979-09-02       Impact factor: 4.132

9.  13S+. Giant satellites or de novo rearrangement?

Authors:  K Imaizumi; T Kajii; N Niikawa
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

10.  A paternal t(6;22)(q25.3;p12) leading to a deleted and satellited der(6) in a short-lived infant.

Authors:  María Guadalupe Domínguez; Horacio Rivera; Rosa María Dávalos-Pulido; Ingrid Patricia Dávalos-Rodríguez
Journal:  J Clin Lab Anal       Date:  2020-05-12       Impact factor: 2.352

  10 in total

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