Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

L Willatt

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

Pageof 1
Sort By:
Journal of Medical Genetics|July 29, 1999
A neuropsychological-genetic profile of atypical cri du chat syndrome: implications for prognosisK M Cornish, G Cross, A Green, et al.
Journal of Medical Genetics|December 10, 1997
Germline duplication of chromosome 2p and neuroblastomaJ S Patel, J Pearson, L Willatt, et al.
The British Journal of Ophthalmology|February 1, 1991
Flecked retina associated with ring 17 chromosomeS J Charles, A T Moore, B C Davison, et al.
Annales De Genetique|January 1, 1992
Cytogenetic and molecular investigations of an abnormal Y chromosome: evidence for a pseudo-dicentric (Yq) isochromosomeJ B Savary, F Vasseur, M Flactif, et al.
Journal of Medical Genetics|June 9, 2009
17q21.31 microduplication patients are characterised by behavioural problems and poor social interactionB Grisart, L Willatt, A Destrée, et al.
Journal of Medical Genetics|April 3, 2004
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic featuresC Shaw-Smith, R Redon, L Rickman, et al.
Journal of Medical Genetics|January 8, 2009
19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisationV Malan, O Raoul, H V Firth, et al.
Journal of Medical Genetics|June 19, 2002
A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocationI Borg, M Squire, C Menzel, et al.
Journal of Medical Genetics|July 17, 2008
Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD A Koolen, A J Sharp, J A Hurst, et al.
Journal of Medical Genetics|April 18, 2009
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcomeB W M van Bon, H C Mefford, B Menten, et al.
Pageof 1

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

Sort By:
Pageof 1
Journal of Medical Genetics|July 29, 1999
A neuropsychological-genetic profile of atypical cri du chat syndrome: implications for prognosisK M Cornish, G Cross, A Green, et al.
Journal of Medical Genetics|December 10, 1997
Germline duplication of chromosome 2p and neuroblastomaJ S Patel, J Pearson, L Willatt, et al.
The British Journal of Ophthalmology|February 1, 1991
Flecked retina associated with ring 17 chromosomeS J Charles, A T Moore, B C Davison, et al.
Annales De Genetique|January 1, 1992
Cytogenetic and molecular investigations of an abnormal Y chromosome: evidence for a pseudo-dicentric (Yq) isochromosomeJ B Savary, F Vasseur, M Flactif, et al.
Journal of Medical Genetics|June 9, 2009
17q21.31 microduplication patients are characterised by behavioural problems and poor social interactionB Grisart, L Willatt, A Destrée, et al.
Journal of Medical Genetics|April 3, 2004
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic featuresC Shaw-Smith, R Redon, L Rickman, et al.
Journal of Medical Genetics|January 8, 2009
19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisationV Malan, O Raoul, H V Firth, et al.
Journal of Medical Genetics|June 19, 2002
A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocationI Borg, M Squire, C Menzel, et al.
Journal of Medical Genetics|July 17, 2008
Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD A Koolen, A J Sharp, J A Hurst, et al.
Journal of Medical Genetics|April 18, 2009
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcomeB W M van Bon, H C Mefford, B Menten, et al.
Pageof 1