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Crippa, Milena
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1

Long-read sequencing reveals chromothripsis in a molecularl..:

Bestetti, Ilaria ; Crippa, Milena ; Sironi, Alessandra...
Frontiers in Genetics.  15 (2024)  - p. , 2024
Link: https://doi.org/10.3389/..
 
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2

Case report: atypical Silver-Russell syndrome patient with ..:

Vimercati, Alessandro ; Tannorella, Pierpaola ; Orlandini, Eleonora...
Frontiers in Genetics.  14 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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3

A unique Smith-Magenis patient with a de novo intragenic de..:

Sironi, Alessandra ; Bestetti, Ilaria ; Masciadri, Maura...
European Journal of Human Genetics.  30 (2022)  11 - p. 1233-1238 , 2022
Link: https://doi.org/10.1038/..
 
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4

Expanding the Molecular Spectrum of ANKRD11 Gene Defects in..:

Bestetti, Ilaria ; Crippa, Milena ; Sironi, Alessandra...
International Journal of Molecular Sciences.  23 (2022)  11 - p. 5912 , 2022
Link: https://doi.org/10.3390/..
 
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5

A familial t(4;8) translocation segregates with epilepsy an..:

Crippa, Milena ; Malatesta, Paola ; Bonati, Maria Teresa...
Annals of Clinical and Translational Neurology.  7 (2020)  5 - p. 855-859 , 2020
Link: https://doi.org/10.1002/..
 
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6

(Epi)genetic profiling of extraembryonic and postnatal tiss..:

Fontana, Laura ; Bedeschi, Maria F. ; Cagnoli, Giulia A....
Molecular Genetics & Genomic Medicine.  8 (2020)  9 - p. , 2020
Link: https://doi.org/10.1002/..
 
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7

SETD5 Gene Haploinsufficiency in Three Patients With Suspec..:

Crippa, Milena ; Bestetti, Ilaria ; Maitz, Silvia...
Frontiers in Neurology.  11 (2020)  - p. , 2020
Link: https://doi.org/10.3389/..
 
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8

Exploring by whole exome sequencing patients with initial d..:

Negri, Gloria ; Magini, Pamela ; Milani, Donatella...
Human Genetics.  138 (2019)  3 - p. 257-269 , 2019
Link: https://doi.org/10.1007/..
 
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9

9q34.3 microduplications lead to neurodevelopmental disorde..:

Bonati, Maria Teresa ; Castronovo, Chiara ; Sironi, Alessandra...
neurogenetics.  20 (2019)  3 - p. 145-154 , 2019
Link: https://doi.org/10.1007/..
 
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10

Molecular Etiology Disclosed by Array CGH in Patients With ..:

Crippa, Milena ; Bonati, Maria Teresa ; Calzari, Luciano...
Frontiers in Genetics.  10 (2019)  - p. , 2019
Link: https://doi.org/10.3389/..
 
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11

Generation of three iPSC lines (IAIi002, IAIi004, IAIi003) ..:

Alari, Valentina ; Russo, Silvia ; Rovina, Davide...
Stem Cell Research.  40 (2019)  - p. 101553 , 2019
Link: https://doi.org/10.1016/..
 
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12

Generation of the Rubinstein-Taybi syndrome type 2 patient-..:

Alari, Valentina ; Russo, Silvia ; Rovina, Davide...
Stem Cell Research.  30 (2018)  - p. 175-179 , 2018
Link: https://doi.org/10.1016/..
 
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13

Familial intragenic duplication of ANKRD11 underlying three..:

Crippa, Milena ; Rusconi, Daniela ; Castronovo, Chiara...
Molecular Cytogenetics.  8 (2015)  1 - p. , 2015
Link: https://doi.org/10.1186/..
 
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14

From Whole Gene Deletion to Point Mutations ofEP300-Positiv..:

Negri, Gloria ; Magini, Pamela ; Milani, Donatella...
Human Mutation.  37 (2015)  2 - p. 175-183 , 2015
Link: https://doi.org/10.1002/..
 
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15

Constitutional de novo deletion of the FBXW7 gene in a pati..:

Roversi, Gaia ; Picinelli, Chiara ; Bestetti, Ilaria...
Scientific Reports.  5 (2015)  1 - p. , 2015
Link: https://doi.org/10.1038/..
 
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