New insights in phenotype and treatment of lung disease immuno-deficiency and chromosome breakage syndrome (LICS)

Brigitte W.M. Willemse(University Medical Center Groningen), Gijs van Haaften(Utrecht University), Marije P. Hennus(University Medical Center Utrecht), Wim Timens(University Medical Center Groningen), Caroline A. Lindemans(University Medical Center Utrecht), Saskia N. van der Crabben(ERN GUARD-Heart), Jaap Jan Boelens(Wilhelmina Children's Hospital), Wilhelmina S. Kerstjens‐Frederikse(University Medical Center Groningen), Joris M. van Montfrans(Wilhelmina Children's Hospital)
Orphanet Journal of Rare Diseases
March 19, 2021
Cited by 6


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