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Achalasia as the harbinger of a novel mitochondrial disorder in childhood.
Chelimsky G, Shanske S, Hirano M, Zinn AB, Cohen M, McNeeley K, Chelimsky TC. Chelimsky G, et al. Among authors: zinn ab. J Pediatr Gastroenterol Nutr. 2005 Apr;40(4):512-7. doi: 10.1097/01.mpg.0000155185.38754.ee. J Pediatr Gastroenterol Nutr. 2005. PMID: 15795604 No abstract available.
Pendular nystagmus in patients with peroxisomal assembly disorder.
Kori AA, Robin NH, Jacobs JB, Erchul DM, Zaidat OO, Remler BF, Averbuch-Heller L, Dell'Osso LF, Leigh RJ, Zinn AB. Kori AA, et al. Among authors: zinn ab. Arch Neurol. 1998 Apr;55(4):554-8. doi: 10.1001/archneur.55.4.554. Arch Neurol. 1998. PMID: 9561985
Maculopathy in spinocerebellar ataxia type 7.
Morrow MJ, Zinn AB, Tucker T, Leigh RJ. Morrow MJ, et al. Among authors: zinn ab. Neurology. 1999 Jul 13;53(1):244. doi: 10.1212/wnl.53.1.244. Neurology. 1999. PMID: 10408582 No abstract available.
Distal deletion of the short arm of chromosome 6.
Zurcher VL, Golden WL, Zinn AB. Zurcher VL, et al. Among authors: zinn ab. Am J Med Genet. 1990 Feb;35(2):261-5. doi: 10.1002/ajmg.1320350223. Am J Med Genet. 1990. PMID: 2309766
The clinical introduction of genetic testing for Alzheimer disease. An ethical perspective.
Post SG, Whitehouse PJ, Binstock RH, Bird TD, Eckert SK, Farrer LA, Fleck LM, Gaines AD, Juengst ET, Karlinsky H, Miles S, Murray TH, Quaid KA, Relkin NR, Roses AD, St George-Hyslop PH, Sachs GA, Steinbock B, Truschke EF, Zinn AB. Post SG, et al. Among authors: zinn ab. JAMA. 1997 Mar 12;277(10):832-6. doi: 10.1001/jama.277.10.832. JAMA. 1997. PMID: 9052715 Review.
29 results