Occurrence of myeloproliferative disorder in patients with Noonan syndrome

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.

R.Cutler Allen, Huda Y. Zoghbi, A. Moseley et al. · PubMed · 1992 · 1.7K citations

Medicine, Genetics, Molecular Genetics +14

A clinical study of Noonan syndrome.

Mike Sharland, Michael Burch, W M McKenna et al. · Archives of Disease in Childhood · 1992 · 477 citations · Full text

Medicine, Cardiology, Pediatrics +13

Loss of The Normal NF1 Allele from the Bone Marrow of Children with Type 1 Neurofibromatosis and Malignant Myeloid Disorders

Kevin Shannon, P. O’Connell, George A. Martin et al. · New England Journal of Medicine · 1994 · 449 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Associated noncardiac malformations in children with congenital heart disease

Jacqueline A. Noonan · Jornal de Pediatria · 1963 · 390 citations

Medicine, Cardiology, Pediatrics +14

Mapping a gene for Noonan syndrome to the long arm of chromosome 12

C. Ruth Jamieson, Ineke van der Burgt, Angela F. Brady et al. · Nature Genetics · 1994 · 290 citations

Life Sciences, Genetics, Molecular Genetics +9