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P Willner

Showing results (151-160 of 169) with videos related to

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Prenatal Diagnosis|February 1, 1991
Congenital myotonic dystrophy: an often unsuspected cause of severe polyhydramniosA B Levine, K A Eddleman, U Chitkara, et al.
Clinical Genetics|March 31, 1998
Mosaicism for a small supernumerary ring X chromosome in a dysmorphic, growth-retarded male: mos47,XXY/48,XXY, +r(X)S R Manea, I F Gershin, A Babu, et al.
American Journal of Medical Genetics|April 15, 1994
Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G)G M Pastores, F M Santorelli, S Shanske, et al.
Journal of Intellectual Disability Research : JIDR|August 6, 2014
'It's made all of us bond since that course…' - a qualitative study of service users' experiences of a CBT anger management group interventionP MacMahon, B Stenfert Kroese, A Jahoda, et al.
American Journal of Human Genetics|June 13, 1998
Paternal uniparental disomy for chromosome 1 revealed by molecular analysis of a patient with pycnodysostosisB D Gelb, J P Willner, T M Dunn, et al.
Brain Research|November 11, 2010
Analysis of a purported SHANK3 mutation in a boy with autism: clinical impact of rare variant research in neurodevelopmental disabilitiesAlexander Kolevzon, Guiqing Cai, Latha Soorya, et al.
Psychopharmacology|January 1, 1991
Voltammetric evidence that subsensitivity to reward following chronic mild stress is associated with increased release of mesolimbic dopamineJ A Stamford, R Muscat, J J O'Connor, et al.
American Journal of Medical Genetics|February 7, 1998
Prenatal diagnosis of a familial interchromosomal insertion of Y chromosome heterochromatinP Ashton-Prolla, I F Gershin, A Babu, et al.
Nature|October 20, 2006
An almost head-on collision as the origin of two off-centre rings in the Andromeda galaxyD L Block, F Bournaud, F Combes, et al.
Blood|May 1, 2007
Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenitaBlanche P Alter, Gabriela M Baerlocher, Sharon A Savage, et al.
Pageof 17

Showing results (151-160 of 169) with videos related to

Sort By:
Pageof 17
Prenatal Diagnosis|February 1, 1991
Congenital myotonic dystrophy: an often unsuspected cause of severe polyhydramniosA B Levine, K A Eddleman, U Chitkara, et al.
Clinical Genetics|March 31, 1998
Mosaicism for a small supernumerary ring X chromosome in a dysmorphic, growth-retarded male: mos47,XXY/48,XXY, +r(X)S R Manea, I F Gershin, A Babu, et al.
American Journal of Medical Genetics|April 15, 1994
Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G)G M Pastores, F M Santorelli, S Shanske, et al.
Journal of Intellectual Disability Research : JIDR|August 6, 2014
'It's made all of us bond since that course…' - a qualitative study of service users' experiences of a CBT anger management group interventionP MacMahon, B Stenfert Kroese, A Jahoda, et al.
American Journal of Human Genetics|June 13, 1998
Paternal uniparental disomy for chromosome 1 revealed by molecular analysis of a patient with pycnodysostosisB D Gelb, J P Willner, T M Dunn, et al.
Brain Research|November 11, 2010
Analysis of a purported SHANK3 mutation in a boy with autism: clinical impact of rare variant research in neurodevelopmental disabilitiesAlexander Kolevzon, Guiqing Cai, Latha Soorya, et al.
Psychopharmacology|January 1, 1991
Voltammetric evidence that subsensitivity to reward following chronic mild stress is associated with increased release of mesolimbic dopamineJ A Stamford, R Muscat, J J O'Connor, et al.
American Journal of Medical Genetics|February 7, 1998
Prenatal diagnosis of a familial interchromosomal insertion of Y chromosome heterochromatinP Ashton-Prolla, I F Gershin, A Babu, et al.
Nature|October 20, 2006
An almost head-on collision as the origin of two off-centre rings in the Andromeda galaxyD L Block, F Bournaud, F Combes, et al.
Blood|May 1, 2007
Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenitaBlanche P Alter, Gabriela M Baerlocher, Sharon A Savage, et al.
Pageof 17