DOSTÁL, Aleš, Jitka NĚMEČKOVÁ, Renata GAILLYOVÁ, Vladimíra VRANOVÁ, Dita ŽEŽULKOVÁ, Mojmír LEJSKA, Ivo ŠLAPÁK, Zuzana DOSTÁLOVÁ a Petr KUGLÍK. Identification of 2.3-Mb gene Locus for Congenital Aural Atresia in 18q22.3 Deletion: A Case Report Analysed by Comparative Genomic Hybridization. Online. Otology and Neurotology. 2006, roč. 27, č. 3, s. 427-432, 5 s. ISSN 1531-7129. [citováno 2024-04-24] |
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@article{704200, author = {Dostál, Aleš and Němečková, Jitka and Gaillyová, Renata and Vranová, Vladimíra and Žežulková, Dita and Lejska, Mojmír and Šlapák, Ivo and Dostálová, Zuzana and Kuglík, Petr}, article_number = {3}, keywords = {conductive hearing loss; congenital aural atresia; 18q22.3 deletion; comparative genomic hybridization}, language = {eng}, issn = {1531-7129}, journal = {Otology and Neurotology}, title = {Identification of 2.3-Mb gene Locus for Congenital Aural Atresia in 18q22.3 Deletion: A Case Report Analysed by Comparative Genomic Hybridization}, volume = {27}, year = {2006} }
TY - JOUR ID - 704200 AU - Dostál, Aleš - Němečková, Jitka - Gaillyová, Renata - Vranová, Vladimíra - Žežulková, Dita - Lejska, Mojmír - Šlapák, Ivo - Dostálová, Zuzana - Kuglík, Petr PY - 2006 TI - Identification of 2.3-Mb gene Locus for Congenital Aural Atresia in 18q22.3 Deletion: A Case Report Analysed by Comparative Genomic Hybridization JF - Otology and Neurotology VL - 27 IS - 3 SP - 427-432 EP - 427-432 SN - 15317129 KW - conductive hearing loss KW - congenital aural atresia KW - 18q22.3 deletion KW - comparative genomic hybridization N2 - The study describes one 18q deletion syndrome clinical report analysed by comparative genomic hybridization with an overview of 19 other selected 18q deletion syndrome patients presenting congenital aural atresia from 18 published articles and one presented poster on 18q deletion syndrome. ER -
DOSTÁL, Aleš, Jitka NĚMEČKOVÁ, Renata GAILLYOVÁ, Vladimíra VRANOVÁ, Dita ŽEŽULKOVÁ, Mojmír LEJSKA, Ivo ŠLAPÁK, Zuzana DOSTÁLOVÁ a Petr KUGLÍK. Identification of 2.3-Mb gene Locus for Congenital Aural Atresia in 18q22.3 Deletion: A Case Report Analysed by Comparative Genomic Hybridization. Online. \textit{Otology and Neurotology}. 2006, roč.~27, č.~3, s.~427-432, 5 s. ISSN~1531-7129. [citováno 2024-04-24]
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