Donna L. Daentl

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.

Gregory A. Meyers, David A. Day, Rosalie Goldberg et al. · PubMed · 1996 · 170 citations

Femoral hypoplasia — unusual facies syndrome

Donna L. Daentl, David W. Smith, Charles I. Scott et al. · The Journal of Pediatrics · 1975 · 92 citations

Surgical Pathology, Thumb Hypoplasia, Orthopaedic Surgery +1

Increased risk for developmental delay in Saethre-Chotzen syndrome is associated with TWIST deletions: an improved strategy for TWIST mutation screening

Juanliang Cai, Barbara K. Goodman, Ankita Patel et al. · Human Genetics · 2003 · 74 citations

Developmental Anomaly, Developmental Biology, Mendelian Disorder +10

Developmental interrelationships of uridine uptake, nucleotide formation and incorporation into RNA by early mammalian embryos

Donna L. Daentl, Charles J. Epstein · Developmental Biology · 1971 · 72 citations

Biology, Developmental Biology, Nucleotide Formation +7

Calpain III mutation analysis of a heterogeneous limb–girdle muscular dystrophy population

Fan-Li Chou, C. Angelini, Donna L. Daentl et al. · Neurology · 1999 · 70 citations