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J P Willner

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American Journal of Medical Genetics|May 2, 1997
Paternal uniparental disomy for chromosome 14: a case report and reviewP D Cotter, S Kaffe, L D McCurdy, et al.
Annales De Genetique|January 1, 1997
Homozygosity for pericentric inversions of chromosome 9. Prenatal diagnosis of two casesP D Cotter, A Babu, L D McCurdy, et al.
American Journal of Medical Genetics|August 22, 1997
Prenatal detection and molecular characterization of a de novo duplication of the distal long arm of chromosome 19P D Cotter, L D McCurdy, I F Gershin, et al.
American Journal of Medical Genetics|October 26, 1999
Familial patent ductus arteriosus and bicuspid aortic valve with hand anomalies: a novel heart-hand syndromeB D Gelb, J Zhang, R J Sommer, et al.
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.
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.
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.
Journal of Medical Genetics|October 22, 2003
Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type IIIS L Ness, T Ben-Yosef, A Bar-Lev, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
American Journal of Medical Genetics|May 2, 1997
Paternal uniparental disomy for chromosome 14: a case report and reviewP D Cotter, S Kaffe, L D McCurdy, et al.
Annales De Genetique|January 1, 1997
Homozygosity for pericentric inversions of chromosome 9. Prenatal diagnosis of two casesP D Cotter, A Babu, L D McCurdy, et al.
American Journal of Medical Genetics|August 22, 1997
Prenatal detection and molecular characterization of a de novo duplication of the distal long arm of chromosome 19P D Cotter, L D McCurdy, I F Gershin, et al.
American Journal of Medical Genetics|October 26, 1999
Familial patent ductus arteriosus and bicuspid aortic valve with hand anomalies: a novel heart-hand syndromeB D Gelb, J Zhang, R J Sommer, et al.
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.
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.
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.
Journal of Medical Genetics|October 22, 2003
Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type IIIS L Ness, T Ben-Yosef, A Bar-Lev, et al.
Pageof 2