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Author/Creator Geiger, Dan

1. A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis. Issue 7 (20th June 2012)

Authors:
Zivony-Elboum, Yifat; Westbroek, Wendy; Kfir, Nehama; Savitzki, David; Shoval, Yishay; Bloom, Assnat; Rod, Raya; Khayat, Morad; Gross, Bella; Samri, Walid; Cohen, Hector; Sonkin, Vadim; Freidman, Tatiana; Geiger, Dan; Fattal-Valevski, Aviva; Anikster, Yair; Waters, Aoife M; Kleta, Robert; Falik-Z...
Journal:
Journal of medical genetics
Issue:
Volume 49:Issue 7(2012)
Page Start:
462
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Genetic linkage analysis of a large family identifies FIGN as a candidate modulator of reduced penetrance in heritable pulmonary arterial hypertension. Issue 7 (20th March 2019)

Authors:
Puigdevall, Pau; Piccari, Lucilla; Blanco, Isabel; Barberà, Joan Albert; Geiger, Dan; Badenas, Celia; Milà, Montserrat; Castelo, Robert; Madrigal, Irene
Journal:
Journal of medical genetics
Issue:
Volume 56:Issue 7(2019)
Page Start:
481
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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