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Journal of Child Neurology
|
August 24, 2007
Craniodigital syndrome of Scott: clinical and neuroradiological features of a new case
Donatella Milani, Stefano D'Arrigo, Alessandra Erbetta, et al.
Journal of Intellectual Disability Research : JIDR
|
May 16, 2025
A Further Characterisation of the Neuropsychological Profile, Social Perception, and Academic Skills in Sotos Syndrome
Niccolò Butti, Cosimo Urgesi, Alice Decio, et al.
Congenital Anomalies
|
April 3, 2016
Insights into 6q21-q22: Refinement of the critical region for acro-cardio-facial syndrome
Donatella Milani, Giulia Anna Cagnoli, Marco Baccarin, et al.
American Journal of Medical Genetics. Part A
|
January 6, 2005
Anomalies of the kidney and urinary tract are common in de Lange syndrome
Angelo Selicorni, Cinzia Sforzini, Donatella Milani, et al.
American Journal of Medical Genetics. Part A
|
February 1, 2018
Perthes disease: A new finding in Floating-Harbor syndrome
Donatella Milani, Giulietta Scuvera, Marta Gatti, et al.
Italian Journal of Pediatrics
|
April 18, 2015
HOXA genes cluster: clinical implications of the smallest deletion
Lidia Pezzani, Donatella Milani, Francesca Manzoni, et al.
American Journal of Medical Genetics. Part A
|
March 28, 2017
ZC4H2 deletions can cause severe phenotype in female carriers
Cristina Zanzottera, Donatella Milani, Enrico Alfei, et al.
Genes
|
May 4, 2026
<i>STAG1</i>: Bridging the Gap Between Cohesin Complex and Epigenetic Machinery
Tiziano Palazzotti, Giulia Bruna Marchetti, Rosa Maria Alfano, et al.
American Journal of Medical Genetics. Part A
|
December 27, 2016
Is cutis verticis Gyrata-Intellectual Disability syndrome an underdiagnosed condition? A case report and review of 62 cases
Arianna Tucci, Lidia Pezzani, Giulietta Scuvera, et al.
Pediatric Neurology
|
March 18, 2014
Does the co-occurrence of FGFR3 gene mutation in hypochondroplasia, medial temporal lobe dysgenesis, and focal epilepsy suggest a syndrome?
Antonino Romeo, Monica Lodi, Maurizio Viri, et al.
Page
of 14
Search research articles
Search
Showing results (21-30 of 140) with videos related to
Sort By:
Page
of 14
Journal of Child Neurology
|
August 24, 2007
Craniodigital syndrome of Scott: clinical and neuroradiological features of a new case
Donatella Milani, Stefano D'Arrigo, Alessandra Erbetta, et al.
Journal of Intellectual Disability Research : JIDR
|
May 16, 2025
A Further Characterisation of the Neuropsychological Profile, Social Perception, and Academic Skills in Sotos Syndrome
Niccolò Butti, Cosimo Urgesi, Alice Decio, et al.
Congenital Anomalies
|
April 3, 2016
Insights into 6q21-q22: Refinement of the critical region for acro-cardio-facial syndrome
Donatella Milani, Giulia Anna Cagnoli, Marco Baccarin, et al.
American Journal of Medical Genetics. Part A
|
January 6, 2005
Anomalies of the kidney and urinary tract are common in de Lange syndrome
Angelo Selicorni, Cinzia Sforzini, Donatella Milani, et al.
American Journal of Medical Genetics. Part A
|
February 1, 2018
Perthes disease: A new finding in Floating-Harbor syndrome
Donatella Milani, Giulietta Scuvera, Marta Gatti, et al.
Italian Journal of Pediatrics
|
April 18, 2015
HOXA genes cluster: clinical implications of the smallest deletion
Lidia Pezzani, Donatella Milani, Francesca Manzoni, et al.
American Journal of Medical Genetics. Part A
|
March 28, 2017
ZC4H2 deletions can cause severe phenotype in female carriers
Cristina Zanzottera, Donatella Milani, Enrico Alfei, et al.
Genes
|
May 4, 2026
<i>STAG1</i>: Bridging the Gap Between Cohesin Complex and Epigenetic Machinery
Tiziano Palazzotti, Giulia Bruna Marchetti, Rosa Maria Alfano, et al.
American Journal of Medical Genetics. Part A
|
December 27, 2016
Is cutis verticis Gyrata-Intellectual Disability syndrome an underdiagnosed condition? A case report and review of 62 cases
Arianna Tucci, Lidia Pezzani, Giulietta Scuvera, et al.
Pediatric Neurology
|
March 18, 2014
Does the co-occurrence of FGFR3 gene mutation in hypochondroplasia, medial temporal lobe dysgenesis, and focal epilepsy suggest a syndrome?
Antonino Romeo, Monica Lodi, Maurizio Viri, et al.
Page
of 14