Erawati V. Bawle

Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome

Angela L. Duker, Blake C. Ballif, Erawati V. Bawle et al. · European Journal of Human Genetics · 2010 · 320 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Adult and two children with fetal methotrexate syndrome

Erawati V. Bawle, J Conard, Lester Weiss · Teratology · 1998 · 132 citations

Medicine, Obstetrics, Pediatrics +17

Hearing, Language, Speech, Vestibular, and Dentofacial Disorders in Fetal Alcohol Syndrome

Michael W. Church, Frances Eldis, Brian W. Blakley et al. · Alcoholism Clinical and Experimental Research · 1997 · 131 citations

Medicine, Audiology, Otolaryngology +17

Maternal systemic primary carnitine deficiency uncovered by newborn screening: Clinical, biochemical, and molecular aspects

Ayman W. El‐Hattab, Fangyuan Li, Joseph Shen et al. · Genetics in Medicine · 2010 · 109 citations

Medicine, Biochemistry, Pediatrics +16

Memory and Learning in Children with 22q11.2 Deletion Syndrome: Evidence for Ventral and Dorsal Stream Disruption?

Renée Lajiness-O’Neill, Isabelle Beaulieu, Jeffrey B. Titus et al. · Child Neuropsychology · 2005 · 105 citations

Social Sciences, Behavioral Sciences, Psychology +12