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Natural history of rhizomelic chondrodysplasia punctata.
White AL, Modaff P, Holland-Morris F, Pauli RM. White AL, et al. Am J Med Genet A. 2003 May 1;118A(4):332-42. doi: 10.1002/ajmg.a.20009. Am J Med Genet A. 2003. PMID: 12687664
Head circumference of children with Down syndrome (0-36 months).
Palmer CG, Cronk C, Pueschel SM, Wisniewski KE, Laxova R, Crocker AC, Pauli RM. Palmer CG, et al. Am J Med Genet. 1992 Jan 1;42(1):61-7. doi: 10.1002/ajmg.1320420114. Am J Med Genet. 1992. PMID: 1308367
Absence of predictable phenotypic expression in proximal 15q duplications.
Ludowese CJ, Thompson KJ, Sekhon GS, Pauli RM. Ludowese CJ, et al. Clin Genet. 1991 Sep;40(3):194-201. doi: 10.1111/j.1399-0004.1991.tb03076.x. Clin Genet. 1991. PMID: 1773534
Temperament in Williams syndrome.
Tomc SA, Williamson NK, Pauli RM. Tomc SA, et al. Am J Med Genet. 1990 Jul;36(3):345-52. doi: 10.1002/ajmg.1320360321. Am J Med Genet. 1990. PMID: 2363436
Respiratory complications in children with spondyloepiphyseal dysplasia congenita.
Harding CO, Green CG, Perloff WH, Pauli RM. Harding CO, et al. Pediatr Pulmonol. 1990;9(1):49-54. doi: 10.1002/ppul.1950090112. Pediatr Pulmonol. 1990. PMID: 2388781
Optic atrophy, hearing loss, and peripheral neuropathy.
Hagemoser K, Weinstein J, Bresnick G, Nellis R, Kirkpatrick S, Pauli RM. Hagemoser K, et al. Am J Med Genet. 1989 May;33(1):61-5. doi: 10.1002/ajmg.1320330108. Am J Med Genet. 1989. PMID: 2665489 Review.
Mechanism of bone and cartilage maldevelopment in the warfarin embryopathy.
Pauli RM. Pauli RM. Pathol Immunopathol Res. 1988;7(1-2):107-12. doi: 10.1159/000157104. Pathol Immunopathol Res. 1988. PMID: 3222201 No abstract available.
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