scholarly journals Quick-FISH: A Rapid Fluorescence In Situ Hybridization Technique for Molecular Cytogenetic Analysis

BioTechniques ◽  
1998 ◽  
Vol 24 (5) ◽  
pp. 826-830 ◽  
Author(s):  
Sushanta K. Banerjee ◽  
Allan P. Weston ◽  
Diane L. Persons ◽  
Donald R. Campbell
Keyword(s):  
In Situ Hybridization ◽  
Fluorescence In Situ Hybridization ◽  
Cytogenetic Analysis ◽  
Hybridization Technique ◽  
Molecular Cytogenetic

Molecular cytogenetic analysis of Siberian Larix species by fluorescence in situ hybridization

2012 ◽  
Vol 299 (2) ◽  
pp. 471-479 ◽  
Author(s):  
Olga V. Goryachkina ◽  
Ekaterina D. Badaeva ◽  
Elena N. Muratova ◽  
Alexandr V. Zelenin
Keyword(s):  
In Situ Hybridization ◽  
Fluorescence In Situ Hybridization ◽  
Cytogenetic Analysis ◽  
Molecular Cytogenetic

scholarly journals Tetrasomy 15q11-q13 identified by fluorescence in situ hybridization in a patient with autistic disorder

2002 ◽  
Vol 60 (2A) ◽  
pp. 290-294 ◽  
Author(s):  
Ana Elizabete Silva ◽  
Sheila Adami Vayego-Lourenço ◽  
Agnes Cristina Fett-Conte ◽  
Eny Maria Goloni-Bertollo ◽  
Marileila Varella-Garcia
Keyword(s):  
In Situ Hybridization ◽  
Fluorescence In Situ Hybridization ◽  
Autistic Disorder ◽  
Gaba Receptor ◽  
Clinical Symptoms ◽  
Female Child ◽  
Hybridization Technique ◽  
Developmental Problems ◽  
Molecular Cytogenetic

We report a female child with tetrasomy of the 15q11-q13 chromosomal region, and autistic disorder associated with mental retardation, developmental problems and behavioral disorders. Combining classical and molecular cytogenetic approaches by fluorescence in situ hybridization technique, the karyotype was demonstrated as 47,XX,+mar.ish der(15)(D15Z1++,D15S11++,GABRB3++,PML-). Duplication of the 15q proximal segment represents the most consistent chromosomal abnormality reported in association with autism. The contribution of the GABA receptor subunit genes, and other genes mapped to this region, to the clinical symptoms of the disease is discussed.

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