Kenneth N. Rosenbaum
National Hospital(IN)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Connective tissue disorders research, Prenatal Screening and Diagnostics, Chromosomal and Genetic Variations, Congenital heart defects research
Most-Cited Works
- → Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta(2007)480 cited
- → Best Practices in Managing Transition to Adulthood for Adolescents With Congenital Heart Disease: The Transition Process and Medical and Psychosocial Issues(2011)453 cited
- → Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844–848(2017)205 cited
- → Frontometaphyseal dysplasia: Neonatal radiographic diagnosis(1995)193 cited
- → Limb pterygium syndromes: A review and report of eleven patients(1982)173 cited
- → Dominant Mutations in KAT6A Cause Intellectual Disability with Recognizable Syndromic Features(2015)142 cited