scholarly journals Chromosome analysis using different staining techniques and fluorescent in situ hybridization in Cerithium vulgatum (Gastropoda: Cerithiidae)

Hereditas ◽  
2002 ◽  
Vol 137 (2) ◽  
pp. 101-106 ◽  
Author(s):  
R. VITTURI1 ◽  
M. COLOMBA2 ◽  
L. CASTRIOTA3 ◽  
A. M. BELTRANO4 ◽  
A. LANNINO1 ◽  
...  
Keyword(s):  
In Situ Hybridization ◽  
Fluorescent In Situ Hybridization ◽  
Chromosome Analysis ◽  
Staining Techniques

scholarly journals Chlorine-Susceptible and Chlorine-Resistant Type 021N Bacteria Occurring in Bulking Activated Sludges

2001 ◽  
Vol 67 (11) ◽  
pp. 5303-5307 ◽  
Author(s):  
M. A. Séka ◽  
Y. Kalogo ◽  
F. Hammes ◽  
J. Kielemoes ◽  
W. Verstraete
Keyword(s):  
In Situ Hybridization ◽  
Fluorescent In Situ Hybridization ◽  
Morphological Features ◽  
The Other ◽  
Filamentous Bacteria ◽  
Staining Techniques ◽  
Effect Of Chlorine

ABSTRACT Two filamentous bacteria causing bulking in two activated sludges were examined. Investigations using morphological features, staining techniques, and fluorescent in situ hybridization identified both filaments as type 021N. However, an examination of the effect of chlorine on the sludges revealed a chlorine-susceptible type 021N in one sludge and a chlorine-resistant type 021N in the other.

scholarly journals Use of FISH technique in the diagnosis of chromosomal syndromes

1999 ◽  
Vol 5 (6) ◽  
pp. 1218-1224
Author(s):  
M. A. Iqbal ◽  
C. Ulmer ◽  
N. Sakati
Keyword(s):  
In Situ Hybridization ◽  
Fluorescent In Situ Hybridization ◽  
Chromosome Analysis ◽  
Laboratory Diagnosis ◽  
Fish Analysis ◽  
Prader Willi Syndrome ◽  
Microdeletion Syndrome ◽  
Microdeletion Syndromes ◽  
Di George Syndrome

Major chromosome abnormalities are present in 0.65% of all neonates. Fluorescent in situ hybridization [FISH]is useful in diagnosing microdeletion syndromes that would otherwise be difficult to diagnose using standard cytogenetics. In this study, we used FISH analysis in the laboratory diagnosis of 4 patients with Prader-Willi Syndrome [del[15][q11.2q12], 4 patients with Di George syndrome [del[22][q11.2q11.23] and 4 patients with Williams syndrome [del[7][q11.23q11.23]. High-resolution chromosome analysis in all these patients was either normal or inconclusive but all the syndromes were confirmed using FISH. We recommend cytogenetic analysis should always be supplemented with FISH to diagnose all cases suspected of a microdeletion syndrome

Karyotypic characterization of the great sturgeon, Huso huso , by multiple staining techniques and fluorescent in situ hybridization

1998 ◽  
Vol 132 (3) ◽  
pp. 495-501 ◽  
Author(s):  
F. Fontana ◽  
J. Tagliavini ◽  
L. Congiu ◽  
M. Lanfredi ◽  
M. Chicca ◽  
...  
Keyword(s):  
In Situ Hybridization ◽  
Fluorescent In Situ Hybridization ◽  
Huso Huso ◽  
Great Sturgeon ◽  
Staining Techniques

1796: Analysis of Chromosomal Aneuploidy in Patients with Oligoasthenoteratozoospermia(OAT) Using Fluorescent in-situ Hybridization

2007 ◽  
Vol 177 (4S) ◽  
pp. 596-597
Author(s):  
Joseph P. Alukal ◽  
Bobby B. Najari ◽  
Wilson Chuang ◽  
Lata Murthy ◽  
Monica Lopez-Perdomo ◽  
...  
Keyword(s):  
In Situ Hybridization ◽  
Fluorescent In Situ Hybridization ◽  
Chromosomal Aneuploidy
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