Frank Greenberg
Publications by Year
Research Areas
Prenatal Screening and Diagnostics, Genomic variations and chromosomal abnormalities, Genetic Syndromes and Imprinting, Williams Syndrome Research, Congenital heart defects research
Most-Cited Works
- → Prader-Willi Syndrome: Consensus Diagnostic Criteria(1993)1,286 cited
- → Hyper-IgE Syndrome with Recurrent Infections — An Autosomal Dominant Multisystem Disorder(1999)789 cited
- → Diagnostic criteria for Walker‐Warburg syndrome(1989)448 cited
- Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).(1991)
- → Chromosome 1p36 Deletions: The Clinical Phenotype and Molecular Characterization of a Common Newly Delineated Syndrome(1997)342 cited
- → Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)(1996)325 cited
- → A Population Study of the VACTERL Association: Evidence for Its Etiologic Heterogeneity(1983)292 cited
- → Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A(1992)291 cited
- Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndrome.(1995)
- → Syndromes with lissencephaly. I: Millerdieker and Norman‐Roberts syndromes and isolated lissencephaly(1984)218 cited