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Expert Review of Proteomics
|
April 12, 2013
The future of prenatal diagnosis: karyotype, microarray or both? Technical and ethical considerations
Antonio Novelli, Pietro Cavalli, Laura Bernardini
American Journal of Medical Genetics. Part A
|
November 19, 2009
Expanding the phenotype of duplication of the Rubinstein-Taybi region on 16p13.3
Bruno Dallapiccola, Laura Bernardini, Antonio Novelli, et al.
American Journal of Medical Genetics. Part A
|
February 14, 2009
Phenocopy of Wolf-Hirschhorn syndrome in a patient with duplication 12q13.3q14.1
Bruno Dallapiccola, Laura Bernardini, Antonio Novelli, et al.
American Journal of Medical Genetics. Part A
|
August 12, 2016
Spectrum of epilepsy and electroencephalogram patterns in idic (15) syndrome
Agatino Battaglia, Laura Bernardini, Isabella Torrente, et al.
American Journal of Medical Genetics. Part A
|
May 19, 2009
Further characterization of the new microdeletion syndrome of 16p11.2-p12.2
Agatino Battaglia, Antonio Novelli, Laura Bernardini, et al.
Prenatal Diagnosis
|
April 26, 2005
Reproductive history of a healthy woman with mosaic duplication of chromosome 4p
Laura Bernardini, Lorenzo Sinibaldi, Caterina Ceccarini, et al.
Central Nervous System Agents in Medicinal Chemistry
|
August 5, 2016
Alpha-7 Nicotinic Receptors in Nervous System Disorders: From Function to Therapeutic Perspectives
Antonella De Jaco, Laura Bernardini, Jessica Rosati, et al.
Genomics
|
June 18, 2003
Linkage disequilibrium analysis of the human adenosine deaminase (ada) gene provides evidence for a lack of correlation between hot spots of equal and unequal homologous recombination
Fulvio Cruciani, Laura Bernardini, Piero Santolamazza, et al.
European Journal of Human Genetics : EJHG
|
September 8, 2011
Clinical utility gene card for: Mayer-Rokitansky-Küster-Hauser syndrome
Karine Morcel, Bruno Dallapiccola, Laurent Pasquier, et al.
Epilepsy & Behavior Case Reports
|
January 4, 2019
Epilepsy phenotype in patients with Xp22.31 microduplication
Mario Brinciotti, Francesca Fioriello, Antonio Mittica, et al.
Page
of 16
Search research articles
Search
Showing results (1-10 of 157) with videos related to
Sort By:
Page
of 16
Expert Review of Proteomics
|
April 12, 2013
The future of prenatal diagnosis: karyotype, microarray or both? Technical and ethical considerations
Antonio Novelli, Pietro Cavalli, Laura Bernardini
American Journal of Medical Genetics. Part A
|
November 19, 2009
Expanding the phenotype of duplication of the Rubinstein-Taybi region on 16p13.3
Bruno Dallapiccola, Laura Bernardini, Antonio Novelli, et al.
American Journal of Medical Genetics. Part A
|
February 14, 2009
Phenocopy of Wolf-Hirschhorn syndrome in a patient with duplication 12q13.3q14.1
Bruno Dallapiccola, Laura Bernardini, Antonio Novelli, et al.
American Journal of Medical Genetics. Part A
|
August 12, 2016
Spectrum of epilepsy and electroencephalogram patterns in idic (15) syndrome
Agatino Battaglia, Laura Bernardini, Isabella Torrente, et al.
American Journal of Medical Genetics. Part A
|
May 19, 2009
Further characterization of the new microdeletion syndrome of 16p11.2-p12.2
Agatino Battaglia, Antonio Novelli, Laura Bernardini, et al.
Prenatal Diagnosis
|
April 26, 2005
Reproductive history of a healthy woman with mosaic duplication of chromosome 4p
Laura Bernardini, Lorenzo Sinibaldi, Caterina Ceccarini, et al.
Central Nervous System Agents in Medicinal Chemistry
|
August 5, 2016
Alpha-7 Nicotinic Receptors in Nervous System Disorders: From Function to Therapeutic Perspectives
Antonella De Jaco, Laura Bernardini, Jessica Rosati, et al.
Genomics
|
June 18, 2003
Linkage disequilibrium analysis of the human adenosine deaminase (ada) gene provides evidence for a lack of correlation between hot spots of equal and unequal homologous recombination
Fulvio Cruciani, Laura Bernardini, Piero Santolamazza, et al.
European Journal of Human Genetics : EJHG
|
September 8, 2011
Clinical utility gene card for: Mayer-Rokitansky-Küster-Hauser syndrome
Karine Morcel, Bruno Dallapiccola, Laurent Pasquier, et al.
Epilepsy & Behavior Case Reports
|
January 4, 2019
Epilepsy phenotype in patients with Xp22.31 microduplication
Mario Brinciotti, Francesca Fioriello, Antonio Mittica, et al.
Page
of 16