Literature DB >> 26141476

Update and Review: Supernumerary Marker Chromosomes.

S Ungerleider1.   

Abstract

Supernumerary marker chromosomes (SMCs) are found in individuals with normal and abnormal clinical phenotypes. Correlations between karyotype and phenotype have been made in only a few circumstances. This article summarizes the most recent information regarding supernumerary marker chromosomes, including genetic counseling issues.

Year:  2000        PMID： 26141476     DOI： 10.1023/A:1009458230654

Source DB:  PubMed          Journal:  J Genet Couns        ISSN： 1059-7700            Impact factor:   2.537


  51 in total

1.  Familial supernumerary chromosome and malignancy.

Authors:  J M Milunsky; H E Wyandt; A Milunsky
Journal:  Cancer Genet Cytogenet       Date:  1996-07-15

2.  De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints.

Authors:  D Warburton
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

3.  Rapid identification of marker chromosomes using primed in situ labeling (PRINS).

Authors:  G V Velagaleti; S A Tharapel; P R Martens; A T Tharapel
Journal:  Am J Med Genet       Date:  1997-08-08

4.  Characterization of a small supernumerary ring X chromosome by fluorescence in situ hybridization.

Authors:  A M Duncan; A Macdonald; C J Brown; D Wolff; H F Willard; B Sutton
Journal:  Am J Med Genet       Date:  1993-12-01

5.  Delineation of supernumerary marker chromosomes in 38 patients.

Authors:  R Viersbach; H Engels; U Gamerdinger; M Hansmann
Journal:  Am J Med Genet       Date:  1998-04-01

6.  Determinants of parental decision to abort or continue after non-aneuploid ultrasound-detected fetal abnormalities.

Authors:  P G Pryde; N B Isada; M Hallak; M P Johnson; A E Odgers; M I Evans
Journal:  Obstet Gynecol       Date:  1992-07       Impact factor: 7.661

7.  Deletion breakpoints associated with the Prader-Willi and Angelman syndromes (15q11-q13) are not sites of high homologous recombination.

Authors:  W P Robinson; R Spiegel; A A Schinzel
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

8.  Identification of an unusual marker chromosome by spectral karyotyping.

Authors:  B Huang; Y Ning; A N Lamb; C J Sandlin; M Jamehdor; T Ried; J Bartley
Journal:  Am J Med Genet       Date:  1998-12-04

9.  Screening for Y-derived sex determining gene SRY in 40 patients with Turner syndrome.

Authors:  R Medlej; J M Lobaccaro; P Berta; C Belon; B Leheup; J E Toublanc; J Weill; C Chevalier; R Dumas; C Sultan
Journal:  J Clin Endocrinol Metab       Date:  1992-11       Impact factor: 5.958

10.  The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture.

Authors:  A Schinzel; W Schmid; M Fraccaro; L Tiepolo; O Zuffardi; J M Opitz; J Lindsten; P Zetterqvist; H Enell; C Baccichetti; R Tenconi; R A Pagon
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.