Murray Feingold
Boston Children's Hospital(US)
Publications by Year
Research Areas
Cleft Lip and Palate Research, Craniofacial Disorders and Treatments, Congenital limb and hand anomalies, Metabolism and Genetic Disorders, Congenital Anomalies and Fetal Surgery
Most-Cited Works
- → Novel HOXA13 Mutations and the Phenotypic Spectrum of Hand-Foot-Genital Syndrome(2000)263 cited
- → Mutations in the pre-replication complex cause Meier-Gorlin syndrome(2011)250 cited
- → Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis(2003)240 cited
- → Genetic Heterogeneity of Saethre-Chotzen Syndrome, Due to TWIST and FGFR Mutations(1998)218 cited
- Normal values for selected physical parameters: an aid to syndrome delineation.(1974)
- → Ocular Aspects of Goldenhar's Syndrome(1973)182 cited
- FGFR2 exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: evidence for missense changes, insertions, and a deletion due to alternative RNA splicing.(1996)