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Author/Creator Mila, Montserrat

1. An exome‐wide exploration of cases of primary ovarian insufficiency uncovers novel sequence variants and candidate genes. Issue 3 (28th July 2020)

Authors:
Alvarez‐Mora, Maria Isabel; Todeschini, Anne‐Laure; Caburet, Sandrine; Perets, Lilach Peled; Mila, Montserrat; Younis, Johnny S.; Shalev, Stavit; Veitia, Reiner A.
Journal:
Clinical genetics
Issue:
Volume 98:Issue 3(2020)
Page Start:
293
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Fragile X‐associated tremor/ataxia syndrome: Regional decrease of mitochondrial DNA copy number relates to clinical manifestations. (24th May 2019)

Authors:
Alvarez‐Mora, Maria I.; Podlesniy, Petar; Gelpi, Ellen; Hukema, Renate; Madrigal, Irene; Pagonabarraga, Javier; Trullas, Ramon; Mila, Montserrat; Rodriguez‐Revenga, Laia
Journal:
Genes, brain, and behavior
Issue:
Volume 18:Number 5(2019)
Page Start:
n/a
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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