IGF-I levels in prepubertal and pubertal children with Down syndrome.

Lanfranco F , Valetto Mr , Colabucci F , Proto C
Minerva Endocrinologica 23 ( 2) 31 -36

9
1998
Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndrome

Fatima Abidi , Jérôme Belougne , Corrado Romano , Charles Schwartz
Journal of Medical Genetics 36 ( 3) 183 -186

23
1999
Communicative and cognitive functioning in Angelman syndrome with UBE3A mutation: a case report

Rosa Zuccarello , Corrado Romano , Pinella Failla , Maurizio Elia
Life Span and Disability 15 ( 1) 55 -67

1
2012
A new family with Papillon-Lefèvre syndrome: effectiveness of etretinate treatment.

Dario Batolo , Carmelo Schepis , Maddalena Siragusa , Corrado Romano
Cutis 65 ( 3) 151 -155

33
2000
"Balanced" complex rearrangements: how many are really balanced?

Joris Robert Vermeesch , Liesbeth Backs , Manuela De Gregori , Roberto Ciccone
Chromosome Research 15 19 -19

2007
Effect of hexarelin on growth hormone secretion in Down syndrome

Romano Deghenghi , Maria Rosa Valetto , Fabio Colabucci , Caterina Proto
Developmental Brain Dysfunction 9 ( 4) 204 -210

1996
Further data suggesting IGFBP-3 unreliability for the diagnosis of growth hormone deficiency in Down syndrome

Fabio Colabucci , Caterina Proto , Corrado Romano , Antonino Alberti
Developmental Brain Dysfunction 10 ( 1) 15 -19

1997
Growth hormone releasing activity of hexarelin in Down syndrome

Ezio Ghigo , Bruno P. Imbimbo , Antonino Alberti , Letizia Ragusa
Developmental Brain Dysfunction 9 133 -137

2
1996
Growth hormone and sleep in Down syndrome

Stefano Del Gracco , Sebastiano A. Musumeci , Maria C. Stefanini , Corrado Romano
Developmental Brain Dysfunction 9 114 -120

2
1996
GPR56 gene down-regulation in patients with Klinefelter syndrome: a candidate for infertility?

Sandro La Vignera , Rossella Cannarella , Angela Cordella , Aldo E Calogero
Minerva Endocrinologica

2020
The relevance of deep genomic analyses in families with variably expressive CNVs in the era of personalized medicine

Lucilla Pizzo , Els Voorhoeve , Matthew Jensen , Emily Huber
Molecular Genetics and Metabolism 132

2021
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.

Madelyn A Gillentine , Tianyun Wang , Kendra Hoekzema , Jill Rosenfeld
Genome Medicine 13 ( 1) 63 -63

33
2021
8p23.2-pter Microdeletions: Seven New Cases Narrowing the Candidate Region and Review of the Literature.

Francesca Forzano , Enrico Grosso , Ornella Galesi , Silvana Briuglia
Genes 12 ( 5) 652

2021
Prader-Willi Syndrome with Angelman Syndrome in the Offspring.

Donatella Greco , Corrado Romano , Mirella Vinci , Michele Roccella
Medicina-buenos Aires 57 ( 5) 460

2021
Medial Telangiectatic Sacral Nevi (Types A and C) Associated with Williams Syndrome

Carmelo Schepis , Donatella Greco , Paolo Bosco , Angela Ragusa
Dermatology 201 ( 3) 285 -286

2
2000
33
2019