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Journal of Cellular Physiology
|
December 26, 2006
Optimization of in vitro expansion of human multipotent mesenchymal stromal cells for cell-therapy approaches: further insights in the search for a fetal calf serum substitute
M E Bernardo, M A Avanzini, C Perotti, et al.
Neurogenetics
|
October 16, 2008
Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome)
C D Coldren, Z Lai, P Shragg, et al.
Journal of Medical Genetics
|
November 17, 2007
Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation
E Rossi, M Riegel, J Messa, et al.
Clinical Genetics
|
April 5, 2011
Identification of de novo mutations and rare variants in hypoplastic left heart syndrome
M Iascone, R Ciccone, L Galletti, et al.
Human Genetics
|
January 1, 1981
Preferential maternal derivation in inv dup(15): analysis of eight new cases
P Maraschio, O Zuffardi, F Bernardi, et al.
Italian Journal of Pediatrics
|
March 11, 2018
Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies
I Maini, I Ivanovski, O Djuric, et al.
Clinical Genetics
|
May 31, 2017
Diagnostic application of a capture based NGS test for the concurrent detection of variants in sequence and copy number as well as LOH
A Vetro, D Goidin, I Lesende, et al.
Human Reproduction (Oxford, England)
|
October 2, 2004
Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B
S Bione, F Rizzolio, C Sala, et al.
Neurology
|
December 17, 2008
Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletion
C Cardoso, A Boys, E Parrini, et al.
Human Molecular Genetics
|
April 18, 1998
The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region
L Dal Zotto, N A Quaderi, R Elliott, et al.
Page
of 16
Search research articles
Search
Showing results (141-150 of 159) with videos related to
Sort By:
Page
of 16
Journal of Cellular Physiology
|
December 26, 2006
Optimization of in vitro expansion of human multipotent mesenchymal stromal cells for cell-therapy approaches: further insights in the search for a fetal calf serum substitute
M E Bernardo, M A Avanzini, C Perotti, et al.
Neurogenetics
|
October 16, 2008
Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome)
C D Coldren, Z Lai, P Shragg, et al.
Journal of Medical Genetics
|
November 17, 2007
Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation
E Rossi, M Riegel, J Messa, et al.
Clinical Genetics
|
April 5, 2011
Identification of de novo mutations and rare variants in hypoplastic left heart syndrome
M Iascone, R Ciccone, L Galletti, et al.
Human Genetics
|
January 1, 1981
Preferential maternal derivation in inv dup(15): analysis of eight new cases
P Maraschio, O Zuffardi, F Bernardi, et al.
Italian Journal of Pediatrics
|
March 11, 2018
Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies
I Maini, I Ivanovski, O Djuric, et al.
Clinical Genetics
|
May 31, 2017
Diagnostic application of a capture based NGS test for the concurrent detection of variants in sequence and copy number as well as LOH
A Vetro, D Goidin, I Lesende, et al.
Human Reproduction (Oxford, England)
|
October 2, 2004
Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B
S Bione, F Rizzolio, C Sala, et al.
Neurology
|
December 17, 2008
Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletion
C Cardoso, A Boys, E Parrini, et al.
Human Molecular Genetics
|
April 18, 1998
The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region
L Dal Zotto, N A Quaderi, R Elliott, et al.
Page
of 16