Related Books
Language: en
Pages: 711
Pages: 711
Type: BOOK - Published: 2013-01-29 - Publisher: Springer Science & Business Media
Neurofibromatosis type 1 (NF1), caused by mutational inactivation of the NF1 tumour suppressor gene, is one of the most common dominantly inherited human disord
Language: en
Pages: 0
Pages: 0
Type: BOOK - Published: 2010-12-02 - Publisher: CreateSpace
1 in 3000 people are born with Neurofibromatosis. It affects all of us in different ways. For some, Neurofibromatosis is as clear as the tumors on their face. F
Language: en
Pages: 274
Pages: 274
Type: BOOK - Published: 2018-12-21 - Publisher: Springer
This Atlas of Inherited Retinal Disorders provides a thorough overview of various inherited retinal dystrophies with emphasis on phenotype characteristics and h
Language: en
Pages: 346
Pages: 346
Type: BOOK - Published: 2019-12-06 - Publisher: Springer Nature
This book, now in a second revised edition, casts light on the often complex diagnosis of musculoskeletal tumors and tumor-like conditions by drawing on the exp
Language: en
Pages: 1672
Pages: 1672
Type: BOOK - Published: 2004 - Publisher:
New edition, completely rewritten, with new chapters on endovascular surgery and mitochrondrial and ion channel disorders.