Chinese patient with neurofibromatosis-Noonan syndrome caused by novel heterozygous NF1 exons 1–58 deletion: a case report

Ítems similars

• Chinese patient with neurofibromatosis-Noonan syndrome caused by novel heterozygous NF1 exons 1–58 deletion: a case report
  per: Zhang, Zhen, et al.
  Publicat: (2020)
• A Rare Cause of Pheochromocytoma; Neurofibromatosis Type 1-Noonan Syndrome
  per: Mazhar Müslüm Tuna, et al.
  Publicat: (2014-09-01)
• A Neurofibromatosis Noonan Syndrome Patient Presenting with Abnormal External Genitalia
  per: Esra Işık, et al.
  Publicat: (2020-03-01)
• Tandem duplication within a neurofibromatosis type 1 (NF1) gene exon in a family with features of Watson syndrome and Noonan syndrome.
  per: Tassabehji, M, et al.
  Publicat: (1993)
• NF1 Gene Mutations Represent the Major Molecular Event Underlying Neurofibromatosis-Noonan Syndrome
  per: De Luca, Alessandro, et al.
  Publicat: (2005)