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Hirschsprung's disease and congenital deafness. Familial assocation.
Weinberg AG, Currarino G, Besserman AM. Weinberg AG, et al. Hum Genet. 1977 Sep 22;38(2):157-61. doi: 10.1007/BF00527397. Hum Genet. 1977. PMID: 908562
Genetic heterogeneity in spondyloepiphyseal dysplasia congenita.
Harrod MJ, Friedman JM, Currarino G, Pauli RM, Langer LO Jr. Harrod MJ, et al. Am J Med Genet. 1984 Jun;18(2):311-20. doi: 10.1002/ajmg.1320180215. Am J Med Genet. 1984. PMID: 6431817
A "new" lethal multiple congenital anomaly syndrome: joint contractures, cerebellar hypoplasia, renal hypoplasia, urogenital anomalies, tongue cysts, shortness of limbs, eye abnormalities, defects of the heart, gallbladder agenesis, and ear malformations.
Rutledge JC, Friedman JM, Harrod MJ, Currarino G, Wright CG, Pinckney L, Chen H. Rutledge JC, et al. Am J Med Genet. 1984 Oct;19(2):255-64. doi: 10.1002/ajmg.1320190208. Am J Med Genet. 1984. PMID: 6507477
Causes of congenital unilateral pulmonary hypoplasia: a study of 33 cases.
Currarino G, Williams B. Currarino G, et al. Pediatr Radiol. 1985;15(1):15-24. doi: 10.1007/BF02387847. Pediatr Radiol. 1985. PMID: 3969292
Unilateral absence of thigh muscles confirmed by CT scan.
Peterson JE, Currarino G. Peterson JE, et al. Pediatr Radiol. 1981;11(3):157-9. doi: 10.1007/BF00971820. Pediatr Radiol. 1981. PMID: 7322654
Osteomyelitis of the cervical spine following dental extraction.
Pinckney LE, Currarino G, Highgenboten CL. Pinckney LE, et al. Radiology. 1980 May;135(2):335-7. doi: 10.1148/radiology.135.2.7367624. Radiology. 1980. PMID: 7367624
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