E-LIB Suche - Ergebnisse für: Tassano, E.

1

Scoliosis with cognitive impairment in a girl with 8q11.21q..:

Tassano, E. ; Ronchetto, P. ; Severino, M....
Bone. 150 (2021) - p. 116022 , 2021

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

2

17q23.3 de novo microdeletion involving only TANC2 gene: A ..:

Tassano, E. ; Accogli, A. ; Ronchetto, P....
European Journal of Medical Genetics. 63 (2020) 12 - p. 104094 , 2020

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

3

Structural brain anomalies in Cri-du-Chat syndrome: MRI fin..:

Villa, R. ; Fergnani, V.G.C. ; Silipigni, R....
European Journal of Paediatric Neurology. 28 (2020) - p. 110-119 , 2020

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

4

Clinical and molecular delineation of a 16p13.2p13.13 micro..:

Tassano, E. ; Alpigiani, M.G. ; Calcagno, A....
European Journal of Medical Genetics. 58 (2015) 3 - p. 194-198 , 2015

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

5

Interstitial deletion 14q31.1q31.3 transmitted from a mothe..:

Gimelli, S. ; Cuoco, C. ; Ronchetto, P...
Journal of Applied Genetics. 54 (2013) 3 - p. 361-365 , 2013

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

6

Pituitary deficiency and congenital infiltrating lipomatosi..:

Capra, V. ; Severino, M. ; Rossi, A....
American Journal of Medical Genetics Part A. 164 (2013) 2 - p. 495-499 , 2013

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

7

De novo 13q31.1–q32.1 interstitial deletion encompassing th..:

Tassano, E. ; Di Rocco, M. ; Signa, S..
American Journal of Medical Genetics Part A. 161 (2013) 4 - p. 894-896 , 2013

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

8

Molecular cytogenetic characterization of the first reporte..:

Tassano, E. ; Alpigiani, M.G. ; Salvati, P....
Gene. 511 (2012) 2 - p. 338-340 , 2012

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

9

LONGITUDINAL CONTRACTION OF LEFT VENTRICLE WITH INOTROPIC S..:

Tassano, E. ; Garcia, E. ; Obregon, R....
Echocardiography. 21 (2004) 2 - p. 206-206 , 2004

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

10

Structural brain anomalies in Cri-du-Chat syndrome: MRI fin..:

Villa R ; Fergnani V. G. C ; Silipigni R...
info:eu-repo/semantics/altIdentifier/pmid/32800423. , 2020

Link: http://hdl.handle.net/24..

11

Loss of tubulin deglutamylase CCP1 causes infantile-onset n..:

Shashi, V ; Magiera, M.M ; Klein, D...
info:eu-repo/semantics/altIdentifier/doi/10.15252/embj.2018100540. , 2018

Link: https://push-zb.helmholt..

12

Genotype-phenotype correlation of 2q37 deletions including ..:

Tassano, E ; Buttgereit, J ; Bader, M...
http://edoc.mdc-berlin.de/13160/1/13160oa.pdf. , 2013

Link: http://edoc.mdc-berlin.d..

13

A new recurrent chromosome change in pediatric therapy-rela..:

Tassano E ; Tavella E ; Micalizzi, Cuoco...
info:eu-repo/semantics/altIdentifier/pmid/22616618. , 2012

Link: http://hdl.handle.net/11..

14

Clonal chromosome anomalies and propensity to myeloid malig..:

MASERATI, EMANUELA ; VALLI, ROBERTO ; PRESSATO, BARBARA...
info:eu-repo/semantics/altIdentifier/pmid/18519517. , 2008

Link: http://hdl.handle.net/11..

15

PD-0499 Optimising cervix brachytherapy planning using OAR ..:

Tassano-Smith, E. ; Palmer, A.L. ; Polak, W.
Radiotherapy and Oncology. 182 (2023) - p. S407-S408 , 2023

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