Literature DB >> 6759619

Complex chromosomal rearrangements (CCR) and their genetic consequences.

A Kleczkowska, J P Fryns, H Van den Berghe.   

Abstract

Mesh：

Year:  1982        PMID： 6759619

Source DB:  PubMed          Journal:  J Genet Hum        ISSN： 0021-7743


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  25 in total

1.  Partial trisomy for 5q and monosomy for 12p in a liveborn child as a result of a complex five breakpoint chromosome rearrangement in a parent.

Authors:  C J Van Der Burgt; G F Merkx; A H Janssen; J C Mulder; R F Suijkerbuijk; D F Smeets
Journal:  J Med Genet       Date:  1992-10       Impact factor: 6.318

2.  De novo complex chromosome rearrangement in identical twins with multiple congenital anomalies.

Authors:  Y Wakita; K Narahara; K Tsuji; Y Yokoyama; S Ninomiya; R Murakami; K Kikkawa; Y Seino
Journal:  Hum Genet       Date:  1992-03       Impact factor: 4.132

3.  Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs.

Authors:  D Wieczorek; H Engels; R Viersbach; B Henke; G Schwanitz; E Passarge
Journal:  J Med Genet       Date:  1998-07       Impact factor: 6.318

4.  Diagnosis of a complex chromosomal rearrangement using fluorescent in situ hybridisation.

Authors:  R Wallerstein; L Gibas; C E Anderson; L Jackson
Journal:  J Med Genet       Date:  1996-09       Impact factor: 6.318

5.  Familial complex chromosome rearrangement ascertained by in situ hybridisation.

Authors:  C Fuster; L Miguez; R Miró; M A Rigola; A Perez; J Egozcue
Journal:  J Med Genet       Date:  1997-02       Impact factor: 6.318

6.  Familial four breakpoint complex chromosomal rearrangement as a cause of monosomy 9p22-->pter and trisomy 10p11.2-->pter and 11q21 analysed by dual and triple colour FISH.

Authors:  P Stankiewicz; E Kostyk; E Bocian; H Stańczak; J Parczewska; E Piatkowska; T Mazurczak; J J Pietrzyk
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

7.  Familial complex chromosome rearrangement (CCR) involving 5 breakpoints on chromosomes 1, 3 and 13 in a severe oligozoospermic patient.

Authors:  Lin Li; Xueyuan Heng; Wang Yun; Shuqi Zheng; Jixia Zhang; Wufang Fan
Journal:  J Assist Reprod Genet       Date:  2013-02-05       Impact factor: 3.412

8.  Complex chromosomal rearrangement and multiple spontaneous abortions.

Authors:  J L Gorski; B S Emanuel; E H Zackai; M Mennuti
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132

9.  Application of molecular cytogenetic techniques to clarify apparently balanced complex chromosomal rearrangements in two patients with an abnormal phenotype: case report.

Authors:  Paula Jp de Vree; Marleen Eh Simon; Marieke F van Dooren; Gerda Ht Stoevelaar; José Tw Hilkmann; Michel A Rongen; Gido Cm Huijbregts; Annemieke Jmh Verkerk; Pino J Poddighe
Journal:  Mol Cytogenet       Date:  2009-07-13       Impact factor: 2.009

10.  Identification of a rare de novo three-way complex t(5;20;8)(q31;p11.2;p21) with microdeletions on 5q31.2, 5q31.3, and 8p23.2 in a patient with hearing loss and global developmental delay: case report.

Authors:  Roland Haj; Kelly Jackson; Beth A Torchia; Lisa G Shaffer; Bassem A Bejjani; Gordon C Gowans; Michael W Ruff
Journal:  Mol Cytogenet       Date:  2009-01-07       Impact factor: 2.009
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