Literature DB >> 25809207

Familial hypochondroplasia and acanthosis nigricans with FGFR3 K650T mutation.

M A Cossiez Cacard1, J Coulombe2, P Bernard3, N Kaci4, J M Bressieux5, P F Souchon1, J Motte1, L Legeai-Mallet4, S Hadj-Rabia2,4, C Eschard3.   

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Year:  2015        PMID： 25809207     DOI： 10.1111/jdv.13061

Source DB:  PubMed          Journal:  J Eur Acad Dermatol Venereol        ISSN： 0926-9959            Impact factor:   6.166


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  3 in total

Review 1.  Achondroplasia: a comprehensive clinical review.

Authors:  Richard M Pauli
Journal:  Orphanet J Rare Dis       Date:  2019-01-03       Impact factor: 4.123

Review 2.  Acanthosis nigricans in a Chinese girl with FGFR3 K650 T mutation: a case report and literature review.

Authors:  Junling Fu; Yiting Zhao; Tong Wang; Qian Zhang; Xinhua Xiao
Journal:  BMC Med Genet       Date:  2019-01-11       Impact factor: 2.103

3.  Acanthosis nigricans in a Japanese boy with hypochondroplasia due to a K650T mutation in FGFR3.

Authors:  Hiroki Hirai; Junpei Hamada; Kosei Hasegawa; Eiichi Ishii
Journal:  Clin Pediatr Endocrinol       Date:  2017-09-28
  3 in total

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