Literature DB >> 15354330

FISH analysis helps identify low-level mosaicism in Ullrich-Turner syndrome patients.

Anne Wiktor1, Daniel L Van Dyke.   

Abstract

PURPOSE: To search for X or Y chromosome mosaicism in 45,X individuals using fluorescent in situ hybridization (FISH).
METHODS: From our series of 53 Ullrich-Turner syndrome patients, we used interphase FISH to evaluate the 19 who had an apparently nonmosaic 45,X karyotype with G-banding.
RESULTS: Of those 19 patients, mosaicism was detected in seven (37%), five patients had an XX line, one had a monocentric isochromosome X, and one had a dicentric isochromosome X. No Y chromosome mosaic was identified.
CONCLUSION: FISH analysis is a sensitive and cost-effective adjunct to karyotype analysis to identify sex chromosome mosaicism in UTS.

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Year:  2004        PMID: 15354330     DOI: 10.1097/01.gim.0000127270.49902.56

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  8 in total

1.  Neuro-functional differences associated with arithmetic processing in Turner syndrome.

Authors:  Shelli R Kesler; Vinod Menon; Allan L Reiss
Journal:  Cereb Cortex       Date:  2005-08-31       Impact factor: 5.357

2.  Turner syndrome mosaicism: an unusual case with a de novo large dicentric marker chromosome: mos 45,X/46,X, ter rea(X;X)(p22.3;p22.3).

Authors:  Anna Lisa Nucaro; Paola Melis; Maria Rosaria Casini; Rossano Rossino; Milena Cau; Maria Antonietta Melis; Sandro Loche
Journal:  J Appl Genet       Date:  2008       Impact factor: 3.240

3.  Single-nucleotide polymorphism array genotyping is equivalent to metaphase cytogenetics for diagnosis of Turner syndrome.

Authors:  Siddharth Prakash; Dongchuan Guo; Cheryl L Maslen; Michael Silberbach; Dianna Milewicz; Carolyn A Bondy
Journal:  Genet Med       Date:  2013-06-06       Impact factor: 8.822

4.  45,X mosaicism in northeast China: a clinical report and review of the literature.

Authors:  Xiang-Yin Liu; Hong-Guo Zhang; Shuang Chen; Rui-Xue Wang; Zhi-Hong Zhang; Rui-Zhi Liu
Journal:  J Assist Reprod Genet       Date:  2013-01-09       Impact factor: 3.412

5.  Genetic Investigation of 261 Cases of Turner Syndrome Patients Referred to the Genetic Clinic.

Authors:  Dariush Farhud; Rojiar Asgarian; Amelia Seifalian; Paria Mostafaeinejad; Maryam Eslami
Journal:  Iran J Public Health       Date:  2021-10       Impact factor: 1.429

6.  A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case report.

Authors:  Frenny Sheth; Elisabeth Ewers; Nadezda Kosyakova; Anja Weise; Jayesh Sheth; Manisha Desai; Joris Andrieux; Joris Vermeesch; Ahmed B Hamid; Monika Ziegler; Thomas Liehr
Journal:  Mol Cytogenet       Date:  2009-11-12       Impact factor: 2.009

7.  Chromosome abnormalities in Indonesian patients with short stature.

Authors:  Chrysantine Paramayuda; Hannie Kartapradja; Debby D Ambarwati; Helena W Anggaratri; Lita P Suciati; Nanis S Marzuki; Alida Harahap
Journal:  Mol Cytogenet       Date:  2012-08-06       Impact factor: 2.009

Review 8.  European guidelines for constitutional cytogenomic analysis.

Authors:  Marisa Silva; Nicole de Leeuw; Kathy Mann; Heleen Schuring-Blom; Sian Morgan; Daniela Giardino; Katrina Rack; Ros Hastings
Journal:  Eur J Hum Genet       Date:  2018-10-01       Impact factor: 4.246

  8 in total

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