E-LIB Suche - Ergebnisse für: Garavelli, L.

1

Reconstruction of larval origins based on genetic relatedne..:

Segura-García, I. ; Garavelli, L. ; Tringali, M....
Scientific Reports. 9 (2019) 1 - p. , 2019

Link: https://doi.org/10.1038/..

2

Prematurity, ventricular septal defect and dysmorphisms are..:

Maini, I. ; Ivanovski, I. ; Djuric, O....
Italian Journal of Pediatrics. 44 (2018) 1 - p. , 2018

Link: https://doi.org/10.1186/..

3

Sleep in Mowat-Wilson syndrome (MWS): Clinical and polysomn..:

Ricci, E. ; Di Pisa, V. ; Provini, F....
European Journal of Paediatric Neurology. 21 (2017) - p. e55 , 2017

Link: https://doi.org/10.1016/..

4

Expanding the clinical spectrum of the 'HDAC8-phenotype' - ..:

Parenti, I. ; Gervasini, C. ; Pozojevic, J....
Clinical Genetics. 89 (2016) 5 - p. 564-573 , 2016

Link: https://doi.org/10.1111/..

5

Oral manifestation of Goltz-Gorlin syndrome in a young girl:

Callea, M ; Yavuz, I ; Deroma, L...
Head & Face Medicine. 8 (2012) S1 - p. , 2012

Link: https://doi.org/10.1186/..

6

Modeling the dispersal of Cape hake ichthyoplankton:

Garavelli, L. ; Gruss, A. ; Grote, B....
Journal of Plankton Research. 34 (2012) 8 - p. 655-669 , 2012

Link: https://doi.org/10.1093/..

7

The role of the minor substitutions in the crystal structur..:

Mitolo, D. ; Pinto, D. ; Garavelli, A...
Mineralogy and Petrology. 96 (2009) 1-2 - p. 121-128 , 2009

Link: https://doi.org/10.1007/..

8

Mowat–Wilson syndrome: Facial phenotype changing with age: ..:

Garavelli, L. ; Zollino, M. ; Mainardi, P. Cerruti...
American Journal of Medical Genetics Part A. 149A (2009) 3 - p. 417-426 , 2009

Link: https://doi.org/10.1002/..

9

Mandibuloacral dysplasia type A in childhood:

Garavelli, L. ; D'Apice, M.R. ; Rivieri, F....
American Journal of Medical Genetics Part A. 149A (2009) 10 - p. 2258-2264 , 2009

Link: https://doi.org/10.1002/..

10

Holt–Oram syndrome associated with anomalies of the feet:

Garavelli, L. ; De Brasi, D. ; Verri, R....
American Journal of Medical Genetics Part A. 146A (2008) 9 - p. 1185-1189 , 2008

Link: https://doi.org/10.1002/..

11

The homozygous deletion of the 3′ enhancer of the SHOX gene..:

Bertorelli, R ; Capone, L ; Ambrosetti, F...
Clinical Genetics. 72 (2007) 5 - p. 490-491 , 2007

Link: https://doi.org/10.1111/..

12

Dermatologic Features in Pallister–Killian Syndrome and the..:

GUARESCHI, E ; GARAVELLI, L ; PEDORI, S...
Pediatric Dermatology. 24 (2007) 4 - p. 426-428 , 2007

Link: https://doi.org/10.1111/..

13

Congenital Heart Defects: 15 Years of Experience of the Emi..:

Calzolari, E. ; Garani, G. ; Cocchi, G....
European Journal of Epidemiology. 18 (2003) 8 - p. 773-780 , 2003

Link: https://www.jstor.org/st..

14

Congenital heart defects: 15 years of experience of the Emi..:

Calzolari, E. ; Garani, G. ; Cocchi, G....
European Journal of Epidemiology. 18 (2002) 8 - p. 773-780 , 2002

Link: https://doi.org/10.1023/..

15

Kabuki syndrome and diaphragmatic defects: A frequent assoc..:

Donadio, A. ; Garavelli, L. ; Banchini, G..
American Journal of Medical Genetics. 91 (2000) 2 - p. 164-165 , 2000

Link: https://doi.org/10.1002/..