Sarojini Budden

Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG Hotspots

Mimi Wan, Stephen Sung Jae Lee, Xianyu Zhang et al. · The American Journal of Human Genetics · 1999 · 515 citations · Full text

Genome Instability, Recurrent Spontaneous, Mendelian Disorder +10

Is angelman syndrome an alternate result of del(15)(qllql3)?

R. Ellen Magenis, Michael G. Brown, Deborah A. Lacy et al. · American Journal of Medical Genetics · 1987 · 240 citations

Sleep dysfunction in Rett syndrome: a trial of exogenous melatonin treatment

Angela J. McArthur, Sarojini Budden · Developmental Medicine & Child Neurology · 1998 · 208 citations · Full text

Comparison of the 15q deletions in Prader‐Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences

R.E. Magenis, S Toth-Fejel, Leland Allen et al. · American Journal of Medical Genetics · 1990 · 198 citations

Guidelines for reporting clinical features in cases with MECP2 mutations

Alison Kerr, Yoshiko Nomura, Dawna Armstrong et al. · Brain and Development · 2001 · 146 citations

Genetic Disorder, Genetics, Mecp2 Mutations +7