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Maria Bitner-Glindzicz

Showing results (1-10 of 87) with videos related to

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British Medical Bulletin|September 27, 2002
Hereditary deafness and phenotyping in humansMaria Bitner-Glindzicz
Archives of Disease in Childhood|October 18, 2014
Genetic investigations in childhood deafnessMichael Parker, Maria Bitner-Glindzicz
Postgraduate Medical Journal|July 19, 2015
Republished: Genetic investigations in childhood deafnessMichael Parker, Maria Bitner-Glindzicz
BMJ (Clinical Research Ed.)|October 20, 2007
Ototoxicity caused by aminoglycosidesMaria Bitner-Glindzicz, Shamima Rahman
Archives of Disease in Childhood. Education and Practice Edition|February 11, 2010
Investigation of the child with permanent hearing impairmentBreege Mac Ardle, Maria Bitner-Glindzicz
Archives of Disease in Childhood. Fetal and Neonatal Edition|December 23, 2022
Cumulative risk factors contributing to hearing loss in preterm infantsKathy Chant, Maria Bitner-Glindzicz, Neil Marlow
International Journal of Audiology|March 17, 2007
The changing face of Usher syndrome: clinical implicationsMazal Cohen, Maria Bitner-Glindzicz, Linda Luxon
International Journal of Pediatric Otorhinolaryngology|February 14, 2006
Late postnatal onset of hearing loss due to GJB2 mutationsWaheeda Pagarkar, Maria Bitner-Glindzicz, Jeffrey Knight, et al.
European Journal of Human Genetics : EJHG|May 23, 2013
EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locusLies H Hoefsloot, Anne-Françoise Roux, Maria Bitner-Glindzicz, et al.
Archives of Disease in Childhood. Education and Practice Edition|December 13, 2016
The 100 000 Genomes Project: What it means for paediatricsBlanche H Griffin, Lyn S Chitty, Maria Bitner-Glindzicz
Pageof 9

Showing results (1-10 of 87) with videos related to

Sort By:
Pageof 9
British Medical Bulletin|September 27, 2002
Hereditary deafness and phenotyping in humansMaria Bitner-Glindzicz
Archives of Disease in Childhood|October 18, 2014
Genetic investigations in childhood deafnessMichael Parker, Maria Bitner-Glindzicz
Postgraduate Medical Journal|July 19, 2015
Republished: Genetic investigations in childhood deafnessMichael Parker, Maria Bitner-Glindzicz
BMJ (Clinical Research Ed.)|October 20, 2007
Ototoxicity caused by aminoglycosidesMaria Bitner-Glindzicz, Shamima Rahman
Archives of Disease in Childhood. Education and Practice Edition|February 11, 2010
Investigation of the child with permanent hearing impairmentBreege Mac Ardle, Maria Bitner-Glindzicz
Archives of Disease in Childhood. Fetal and Neonatal Edition|December 23, 2022
Cumulative risk factors contributing to hearing loss in preterm infantsKathy Chant, Maria Bitner-Glindzicz, Neil Marlow
International Journal of Audiology|March 17, 2007
The changing face of Usher syndrome: clinical implicationsMazal Cohen, Maria Bitner-Glindzicz, Linda Luxon
International Journal of Pediatric Otorhinolaryngology|February 14, 2006
Late postnatal onset of hearing loss due to GJB2 mutationsWaheeda Pagarkar, Maria Bitner-Glindzicz, Jeffrey Knight, et al.
European Journal of Human Genetics : EJHG|May 23, 2013
EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locusLies H Hoefsloot, Anne-Françoise Roux, Maria Bitner-Glindzicz, et al.
Archives of Disease in Childhood. Education and Practice Edition|December 13, 2016
The 100 000 Genomes Project: What it means for paediatricsBlanche H Griffin, Lyn S Chitty, Maria Bitner-Glindzicz
Pageof 9