Literature DB >> 7286975

Prenatal detection of an accessory chromosome identified as an inversion duplication (15).

G Stetten, B Sroka-Zaczek, V L Corson.   

Abstract

Mesh：

Year:  1981        PMID： 7286975     DOI： 10.1007/BF00281684

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


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  19 in total

1.  A simple technique for demonstrating centromeric heterochromatin.

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

2.  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

3.  Exclusion of chromosomal mosaicism: tables of 90%, 95% and 99% confidence limits and comments on use.

Authors:  E B Hook
Journal:  Am J Hum Genet       Date:  1977-01       Impact factor: 11.025

4.  Partial trisomy 15 and temporal lobe syndrome in a retarded girl without gross malformations.

Authors:  K Hongell; M Iivanainen
Journal:  Clin Genet       Date:  1978-10       Impact factor: 4.438

5.  Parental origin of de novo chromosome rearrangements.

Authors:  J Chamberlin; R E Magenis
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

6.  Prader-Willi syndrome and a bisatellited derivative of chromosome 15.

Authors:  L P Wisniewski; M E Witt; F Ginsberg-Fellner; J Wilner; R J Desnick
Journal:  Clin Genet       Date:  1980-07       Impact factor: 4.438

7.  A new R-banding technique in clinical cytogenetics.

Authors:  G S Pai; G H Thomas
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

8.  Visualization of nucleolar organizer regions im mammalian chromosomes using silver staining.

Authors:  C Goodpasture; S E Bloom
Journal:  Chromosoma       Date:  1975-11-20       Impact factor: 4.316

9.  Cytogenetic and clinical studies in five cases of inv dup(15).

Authors:  L Wisniewski; T Hassold; J Heffelfinger; J V Higgins
Journal:  Hum Genet       Date:  1979-09       Impact factor: 4.132

10.  Enhancement of banding patterns in human metaphase chromosomes by energy transfer.

Authors:  E Sahar; S A Latt
Journal:  Proc Natl Acad Sci U S A       Date:  1978-11       Impact factor: 11.205
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  14 in total

Review 1.  Chromosome imbalance, normal phenotype, and imprinting.

Authors:  L Bortotto; E Piovan; R Furlan; H Rivera; O Zuffardi
Journal:  J Med Genet       Date:  1990-09       Impact factor: 6.318

2.  Forty four probands with an additional "marker" chromosome.

Authors:  K E Buckton; G Spowart; M S Newton; H J Evans
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

3.  Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes.

Authors:  T A Donlon
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

Review 4.  Inv dup(15) supernumerary marker chromosomes.

Authors:  T Webb
Journal:  J Med Genet       Date:  1994-08       Impact factor: 6.318

5.  Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH).

Authors:  E Blennow; G Annerén; T H Bui; E Berggren; E Asadi; M Nordenskjöld
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

6.  The genetic significance of accessory bisatellited marker chromosomes.

Authors:  P Steinbach; M Djalali; I Hansmann; E Kattner; M Meisel-Stosiek; H D Probeck; A Schmidt; M Wolf
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

7.  Reproductive outcomes of paracentric inversion carriers: report of a liveborn dicentric recombinant and literature review.

Authors:  E H Mules; J Stamberg
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

Review 8.  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

9.  Supernumerary microchromosomes identified as inverted duplications of chromosome 15: a report of three cases.

Authors:  L P Wisniewski; R A Doherty
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

10.  Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.

Authors:  J Leana-Cox; L Jenkins; C G Palmer; R Plattner; L Sheppard; W L Flejter; J Zackowski; F Tsien; S Schwartz
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025
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