1 research outputs found
Improved diagnosis of rare disease patients through systematic detection of runs of homozygosity
- Author
- Ahmet Yaramis
- Alessandra Ferlini
- Alexis Brice
- Alfons Macaya
- Ali Dursun
- Antoni Matilla- Duenas
- Antonia Ribes
- Aurora Pujol
- Beltran S
- Bru Cormand
- Brunhilde Wirth
- Bullich G
- Carlo Rivolta
- Carmen Ayuso
- Carmen Espinós
- Christian Scerri
- Conxi Lázaro
- Daniel Grinberg
- Dilek Yalnizoglu
- Doriette Soler
- Eduardo Tizzano
- Estrella López
- Eva Morava
- Fabrizio Barbetti
- Francesc Cardellach
- Francesc Palau
- Francesca Forzano
- Francesca Mari
- Francesco Muntoni
- Francesco Muntoni
- Frederic Tort
- Gloria Garrabou
- Gonzalo Villanueva
- Henry James Houlden
- Horvath R
- Irene Valenzuela
- Isabel Tejada
- Ivon Cuscó
- Jan Senderek
- Javier Benitez
- Javier Corral De La Calle
- Jordi Serra
- Jose segovia
- José Mª Millán
- Juan Ramon Gimeno Blanes
- Judith Armstrong
- Koksal Ozgul
- Laura Vilarinho
- Laurie S
- Lluis Montoliu
- Lochmüller A
- Manuel Posada
- Maria Antonietta Mencarelli
- Maria Sabater.
- Marina Mora
- Matalonga L
- Mereu E
- Mike Hanna
- Montse Milà
- Paola Bianchi
- Papakonstantinou A
- Pavel Seeman
- Perry M. Elliott
- Pia Gallano
- Piscia D
- Pèrez-Jurado L
- Rafael Artuch
- Ramon Martí Seves
- RD-Connect GPAP and URD-Cat data contributors Alessandra Renieri
- Riess O
- Roser Urreizti
- Sarah Tabrizi
- Semra Hiz Kurul
- Serdal Gungor
- Silvia Vidal
- Susanna Balcells
- Thomas Klockgether
- Thompsom R
- Uluc Yis
- van Ommen GJ
- Vincent Timmerman
- Volker Straub
- Yavuz Oktay
- Publication venue
- Publication date
- 01/01/2020
- Field of study