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 · 316 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +9

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

Dentofacial Disorders, Pediatric Otolaryngology, Audiology +10

Adult and two children with fetal methotrexate syndrome

Erawati V. Bawle, J Conard, Lester Weiss · Teratology · 1998 · 131 citations

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 · 107 citations

Nutrition, Newborn Screening, Pediatrics +8

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 · 103 citations

Developmental Cognitive Neuroscience, Education, Dorsal Stream Disruption +20