Grouping of Multiple-Lentigines/LEOPARD and Noonan Syndromes on the PTPN11 Gene

This publication has 21 references indexed in Scilit:

• Noonan syndrome revisited
  The Journal of Pediatrics, 1999
• Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large family
  European Journal of Human Genetics, 1998
• Multiple lentigines syndrome (LEOPARD syndrome or progressive cardiomyopathic lentiginosis).
  Journal of Medical Genetics, 1997
• Neurofibromatosis type I gene mutation in a patient with features of LEOPARD syndrome
  Human Mutation, 1996
• A Familial Syndrome of Arterial Dissections with Lentiginosis
  New England Journal of Medicine, 1995
• Mapping a gene for Noonan syndrome to the long arm of chromosome 12
  Nature Genetics, 1994
• Cutaneous myxomas. A major component of the complex of myxomas, spotty pigmentation, and endocrine overactivity
  Archives of Dermatology, 1986
• Unifying link between Noonan's and Leopard syndromes?
  Pediatric Cardiology, 1983
• Centrofacial lentiginosis.
  British Journal of Dermatology, 1976
• Pulmonary stenosis, cafe-au-lait spots, and dull intelligence.
  Archives of Disease in Childhood, 1967