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Panagiotis Ν. Krallis
Panagiotis Ν. Krallis
Boston Children's Hospital
Genetics
PLS3
Bone mineral
Osteogenesis imperfecta
Frameshift mutation
2
Papers
14
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Development of a multidisciplinary clinic of neurofibromatosis type 1 and other neurocutaneous disorders in Greece. A 3-year experience
2019
Postgraduate Medicine
Eleftheria Kokkinou
Kleoniki Roka
Alexis Alexopoulos
Efthymia Tsina
Ioannis Nikas
Panagiotis Ν. Krallis
Ioanna Thanopoulou
Lambrini Nasi
Evanthia A. Makrygianni
Eirini Tsoutsou
Konstantina Kosma
Maria Tsipi
Maria Tzetis
Helen Frysira
Antonis Kattamis
Roser Pons
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Citations (3)
A novel frameshift deletion in PLS3 causing severe primary osteoporosis
2018
Journal of Human Genetics
Alice Costantini
Panagiotis Ν. Krallis
Anders Kämpe
Emmanouil M. Karavitakis
Fulya Taylan
Outi Mäkitie
Artemis Doulgeraki
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Citations (11)
1