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Showing results (621-630 of 628) with videos related to

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Journal of Medical Genetics|June 27, 2001
Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformationsE Rossi, F Piccini, M Zollino, et al.
American Journal of Medical Genetics. Part A|March 3, 2005
Mutation analysis of the NSD1 gene in a group of 59 patients with congenital overgrowthM Cecconi, F Forzano, D Milani, et al.
Neurology|November 4, 2006
Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophyE Mercuri, E Bertini, S Messina, et al.
Life Sciences in Space Research|August 14, 2018
A water-filled garment to protect astronauts during interplanetary missions tested on board the ISSG Baiocco, M Giraudo, L Bocchini, et al.
American Journal of Human Genetics|July 20, 2001
p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlationH van Bokhoven, B C Hamel, M Bamshad, et al.
Giornale Italiano Di Medicina Del Lavoro Ed Ergonomia|December 9, 2004
[New biomarkers of exposure]P Apostoli, R Bergonzi, S Catalani, et al.
Human Genetics|January 1, 1982
Cytogenetic findings in 4952 prenatal diagnoses. An Italian collaborative studyG Simoni, M Fraccaro, A Arslanian, et al.
American Journal of Medical Genetics. Part A|February 14, 2009
Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literatureL Garavelli, M Zollino, P Cerruti Mainardi, et al.
Pageof 63

Showing results (621-630 of 628) with videos related to

Sort By:
Pageof 63
You have reached the last page of results.This site can display upto 628 results.
Journal of Medical Genetics|June 27, 2001
Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformationsE Rossi, F Piccini, M Zollino, et al.
American Journal of Medical Genetics. Part A|March 3, 2005
Mutation analysis of the NSD1 gene in a group of 59 patients with congenital overgrowthM Cecconi, F Forzano, D Milani, et al.
Neurology|November 4, 2006
Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophyE Mercuri, E Bertini, S Messina, et al.
Life Sciences in Space Research|August 14, 2018
A water-filled garment to protect astronauts during interplanetary missions tested on board the ISSG Baiocco, M Giraudo, L Bocchini, et al.
American Journal of Human Genetics|July 20, 2001
p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlationH van Bokhoven, B C Hamel, M Bamshad, et al.
Giornale Italiano Di Medicina Del Lavoro Ed Ergonomia|December 9, 2004
[New biomarkers of exposure]P Apostoli, R Bergonzi, S Catalani, et al.
Human Genetics|January 1, 1982
Cytogenetic findings in 4952 prenatal diagnoses. An Italian collaborative studyG Simoni, M Fraccaro, A Arslanian, et al.
American Journal of Medical Genetics. Part A|February 14, 2009
Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literatureL Garavelli, M Zollino, P Cerruti Mainardi, et al.
Pageof 63