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Journal of Pediatric Genetics
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September 13, 2016
Pitt-Hopkins Syndrome and Differential Diagnosis: A Molecular and Clinical Challenge
Giuseppe Marangi, Marcella Zollino
Journal of Human Genetics
|
June 10, 2018
Dissecting the Wolf-Hirschhorn syndrome phenotype: WHSC1 is a neurodevelopmental gene contributing to growth delay, intellectual disability, and to the facial dysmorphism
Marcella Zollino, Paolo Niccolo' Doronzio
European Journal of Human Genetics : EJHG
|
February 24, 2011
Clinical utility gene card for: Mowat-Wilson syndrome
Marcella Zollino, Livia Garavelli, Anita Rauch
American Journal of Medical Genetics. Part A
|
December 25, 2009
Phenotypic map in ring 14 syndrome
Marcella Zollino, Daniela Orteschi, Giovanni Neri
American Journal of Medical Genetics. Part A
|
October 15, 2013
Encomium: Giovanni Neri--polyhedral and down-to-earth mentor
Maurizio Genuardi, Fiorella Gurrieri, Marcella Zollino
European Journal of Medical Genetics
|
May 9, 2012
The ring 14 syndrome
Marcella Zollino, Emanuela Ponzi, Giuseppe Gobbi, et al.
American Journal of Medical Genetics. Part A
|
January 11, 2003
CFC syndrome
Giovanni Neri, Maria Ines Kavamura, Marcella Zollino, et al.
Clinical Linguistics & Phonetics
|
October 13, 2012
Linguistic and psychomotor development in children with chromosome 14 deletions
Laura Zampini, Laura D'Odorico, Paola Zanchi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 25, 2012
Inherited neuropathies and deafness caused by a PMP22 point mutation: a case report and a review of the literature
Marco Luigetti, Marcella Zollino, Guido Conti, et al.
American Journal of Medical Genetics. Part A
|
October 16, 2013
Interstitial deletion of 3p22.3p22.2 encompassing ARPP21 and CLASP2 is a potential pathogenic factor for a syndromic form of intellectual disability: a co-morbidity model with additional copy number variations in a large family
Giuseppe Marangi, Daniela Orteschi, Valentina Milano, et al.
Page
of 16
Search research articles
Search
Showing results (1-10 of 157) with videos related to
Sort By:
Page
of 16
Journal of Pediatric Genetics
|
September 13, 2016
Pitt-Hopkins Syndrome and Differential Diagnosis: A Molecular and Clinical Challenge
Giuseppe Marangi, Marcella Zollino
Journal of Human Genetics
|
June 10, 2018
Dissecting the Wolf-Hirschhorn syndrome phenotype: WHSC1 is a neurodevelopmental gene contributing to growth delay, intellectual disability, and to the facial dysmorphism
Marcella Zollino, Paolo Niccolo' Doronzio
European Journal of Human Genetics : EJHG
|
February 24, 2011
Clinical utility gene card for: Mowat-Wilson syndrome
Marcella Zollino, Livia Garavelli, Anita Rauch
American Journal of Medical Genetics. Part A
|
December 25, 2009
Phenotypic map in ring 14 syndrome
Marcella Zollino, Daniela Orteschi, Giovanni Neri
American Journal of Medical Genetics. Part A
|
October 15, 2013
Encomium: Giovanni Neri--polyhedral and down-to-earth mentor
Maurizio Genuardi, Fiorella Gurrieri, Marcella Zollino
European Journal of Medical Genetics
|
May 9, 2012
The ring 14 syndrome
Marcella Zollino, Emanuela Ponzi, Giuseppe Gobbi, et al.
American Journal of Medical Genetics. Part A
|
January 11, 2003
CFC syndrome
Giovanni Neri, Maria Ines Kavamura, Marcella Zollino, et al.
Clinical Linguistics & Phonetics
|
October 13, 2012
Linguistic and psychomotor development in children with chromosome 14 deletions
Laura Zampini, Laura D'Odorico, Paola Zanchi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 25, 2012
Inherited neuropathies and deafness caused by a PMP22 point mutation: a case report and a review of the literature
Marco Luigetti, Marcella Zollino, Guido Conti, et al.
American Journal of Medical Genetics. Part A
|
October 16, 2013
Interstitial deletion of 3p22.3p22.2 encompassing ARPP21 and CLASP2 is a potential pathogenic factor for a syndromic form of intellectual disability: a co-morbidity model with additional copy number variations in a large family
Giuseppe Marangi, Daniela Orteschi, Valentina Milano, et al.
Page
of 16