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M B Delatycki

Showing results (11-20 of 58) with videos related to

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Clinical Genetics|September 11, 2002
Normal levels of soluble transferrin receptor in Friedreich ataxiaK Sitte, F Zaibak, M B Delatycki, et al.
Prenatal Diagnosis|February 3, 2004
Screening approach for Fragile X syndromeM B Delatycki, L J Sheffield, S Wake, et al.
American Journal of Medical Genetics|February 15, 2001
New variant of familial cerebellar ataxia with hypergonadotropic hypogonadism and sensorineural deafnessD J Amor, M B Delatycki, R J Gardner, et al.
Acta Neurologica Scandinavica|September 29, 2016
A longitudinal study of the SF-36 version 2 in Friedreich ataxiaG Tai, L A Corben, E M Yiu, et al.
Archives of Disease in Childhood|November 23, 2005
Sleep disturbance in Sanfilippo syndrome: a parental questionnaire studyJ Fraser, A A Gason, J E Wraith, et al.
Journal of Child Neurology|December 6, 2001
Genetic factors in athetoid cerebral palsyD J Amor, J E Craig, M B Delatycki, et al.
Public Health Genomics|January 22, 2010
Population-based genetic screening for cystic fibrosis: attitudes and outcomesL Ioannou, J Massie, V Collins, et al.
Journal of Medical Ethics|December 2, 2009
Genetic selection for deafness: the views of hearing children of deaf adultsC Mand, R E Duncan, L Gillam, et al.
Journal of Medical Genetics|August 16, 2003
De novo germline PTEN mutation in a man with Lhermitte-Duclos disease which arose on the paternal chromosome and was transmitted to his child with polydactyly and Wormian bonesM B Delatycki, A Danks, A Churchyard, et al.
Journal of Community Genetics|May 30, 2013
'No thanks'-reasons why pregnant women declined an offer of cystic fibrosis carrier screeningL Ioannou, J Massie, S Lewis, et al.
Pageof 6

Showing results (11-20 of 58) with videos related to

Sort By:
Pageof 6
Clinical Genetics|September 11, 2002
Normal levels of soluble transferrin receptor in Friedreich ataxiaK Sitte, F Zaibak, M B Delatycki, et al.
Prenatal Diagnosis|February 3, 2004
Screening approach for Fragile X syndromeM B Delatycki, L J Sheffield, S Wake, et al.
American Journal of Medical Genetics|February 15, 2001
New variant of familial cerebellar ataxia with hypergonadotropic hypogonadism and sensorineural deafnessD J Amor, M B Delatycki, R J Gardner, et al.
Acta Neurologica Scandinavica|September 29, 2016
A longitudinal study of the SF-36 version 2 in Friedreich ataxiaG Tai, L A Corben, E M Yiu, et al.
Archives of Disease in Childhood|November 23, 2005
Sleep disturbance in Sanfilippo syndrome: a parental questionnaire studyJ Fraser, A A Gason, J E Wraith, et al.
Journal of Child Neurology|December 6, 2001
Genetic factors in athetoid cerebral palsyD J Amor, J E Craig, M B Delatycki, et al.
Public Health Genomics|January 22, 2010
Population-based genetic screening for cystic fibrosis: attitudes and outcomesL Ioannou, J Massie, V Collins, et al.
Journal of Medical Ethics|December 2, 2009
Genetic selection for deafness: the views of hearing children of deaf adultsC Mand, R E Duncan, L Gillam, et al.
Journal of Medical Genetics|August 16, 2003
De novo germline PTEN mutation in a man with Lhermitte-Duclos disease which arose on the paternal chromosome and was transmitted to his child with polydactyly and Wormian bonesM B Delatycki, A Danks, A Churchyard, et al.
Journal of Community Genetics|May 30, 2013
'No thanks'-reasons why pregnant women declined an offer of cystic fibrosis carrier screeningL Ioannou, J Massie, S Lewis, et al.
Pageof 6