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Uniparental disomy in congenital disorders: a prospective study.
Lindor NM, Karnes PS, Michels VV, Dewald GW, Goerss J, Jalal S, Jenkins RB, Vockley G, Thibodeau SN. Lindor NM, et al. Among authors: karnes ps. Am J Med Genet. 1995 Aug 28;58(2):143-6. doi: 10.1002/ajmg.1320580210. Am J Med Genet. 1995. PMID: 8533805
Cytogenetic testing for Williams syndrome.
Jalal SM, Crifasi PA, Karnes PS, Michels VV. Jalal SM, et al. Among authors: karnes ps. Mayo Clin Proc. 1996 Jan;71(1):67-8. doi: 10.4065/71.1.67. Mayo Clin Proc. 1996. PMID: 8538237 No abstract available.
von Hippel-Lindau disease.
Couch V, Lindor NM, Karnes PS, Michels VV. Couch V, et al. Among authors: karnes ps. Mayo Clin Proc. 2000 Mar;75(3):265-72. doi: 10.4065/75.3.265. Mayo Clin Proc. 2000. PMID: 10725953 Review.
New skeletal dysplasia with unique brachydactyly.
Mononen TK, Karnes PS, Senac MO Jr, Falk RE. Mononen TK, et al. Among authors: karnes ps. Am J Med Genet. 1992 Mar 1;42(5):706-13. doi: 10.1002/ajmg.1320420516. Am J Med Genet. 1992. PMID: 1632443
26 results