E-LIB Suche - Ergebnisse für: Divizia, Maria Julia

1

Aprendizaje activo: una propuesta para el estudio del compo..:

Divizia, Maria Julia ; Miranda, A ; Montiveros, L...
info:eu-repo/semantics/altIdentifier/url/https://www.fisica.org.ar/actividades/rafas/libros-de-resumenes/. ,

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

2

Effect of Sanitizers and Glucose on Clostridium perfringens..:

Castro, Melina Gabriela ; Icazatti Zuñiga, Alejandro Ariel ; Divizia, Maria Julia...
info:eu-repo/semantics/altIdentifier/doi/10.20546/ijcmas.2016.507.022. ,

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

3

Abnormalities of pubertal development and gonadal function ..:

Patti, Giuseppa ; Scaglione, Marco ; Maiorano, Nadia Gabriella...
Frontiers in Endocrinology. 14 (2023) - p. , 2023

Link: https://doi.org/10.3389/..

4

An example of parenchymal renal sparing in the context of c..:

Ruscitti, Federica ; Cerminara, Maria ; Iascone, Maria...
Birth Defects Research. 114 (2022) 12 - p. 674-681 , 2022

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

5

Neurodevelopmental Disorders in Patients With Complex Pheno..:

Servetti, Martina ; Pisciotta, Livia ; Tassano, Elisa...
Frontiers in Genetics. 12 (2021) - p. , 2021

Link: https://doi.org/10.3389/..

6

Case Report: Whole Exome Sequencing Revealed Disease-Causin..:

Cerminara, Maria ; Spirito, Giovanni ; Pisciotta, Livia...
Frontiers in Genetics. 12 (2021) - p. , 2021

Link: https://doi.org/10.3389/..

7

Renal involvement and Strømme syndrome:

Caridi, Gianluca ; Lugani, Francesca ; Lerone, Margherita...
Clinical Kidney Journal. 14 (2020) 1 - p. 439-441 , 2020

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

8

Consensus based recommendations for diagnosis and medical m..:

Baldelli, Ilaria ; Baccarani, Alessio ; Barone, Chiara...
Orphanet Journal of Rare Diseases. 15 (2020) 1 - p. , 2020

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

9

Intragenic duplication of KCNQ5 gene results in aberrant sp..:

Rosti, Giulia ; Tassano, Elisa ; Bossi, Simone...
European Journal of Medical Genetics. 62 (2019) 9 - p. 103555 , 2019

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

10

P63 modulates the expression of theWDFY2gene which is impli..:

Monti, Paola ; Ciribilli, Yari ; Foggetti, Giorgia...
Bioscience Reports. 39 (2019) 12 - p. , 2019

Link: https://doi.org/10.1042/..

11

Recurrence and Familial Inheritance of Intronic NIPBL Patho..:

Masciadri, Maura ; Ficcadenti, Anna ; Milani, Donatella...
Frontiers in Neurology. 9 (2018) - p. , 2018

Link: https://doi.org/10.3389/..

12

A multi-method approach to the molecular diagnosis of overt..:

Russo, Silvia ; Calzari, Luciano ; Mussa, Alessandro...
Clinical Epigenetics. 8 (2016) 1 - p. , 2016

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

13

Assessment of copy number variations in 120 patients with P..:

Vaccari, Carlotta Maria ; Tassano, Elisa ; Torre, Michele...
BMC Medical Genetics. 17 (2016) 1 - p. , 2016

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

14

Erratum to: A multi-method approach to the molecular diagno..:

Russo, Silvia ; Calzari, Luciano ; Mussa, Alessandro...
Clinical Epigenetics. 8 (2016) 1 - p. , 2016

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

15

Thrombocytopenia-absent radius (TAR) syndrome due to compou..:

Tassano, Elisa ; Gimelli, Stefania ; Divizia, Maria Teresa...
Molecular Cytogenetics. 8 (2015) 1 - p. , 2015

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