Hoppe DA - Search Results

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Xp22.3 microdeletion syndrome with microphthalmia, sclerocornea, linear skin defects, and congenital heart defects.

Lindor NM, Michels VV, Hoppe DA, Driscoll DJ, Leavitt JA, Dewald GW. Lindor NM, et al. Among authors: hoppe da. Am J Med Genet. 1992 Sep 1;44(1):61-5. doi: 10.1002/ajmg.1320440115. Am J Med Genet. 1992. PMID: 1519653

Absence of chromosome fragility at 19q13.3 in patients with myotonic dystrophy.

Jalal SM, Lindor NM, Michels VV, Buckley DD, Hoppe DA, Sarkar G, Dewald GW. Jalal SM, et al. Among authors: hoppe da. Am J Med Genet. 1993 Jun 1;46(4):441-3. doi: 10.1002/ajmg.1320460419. Am J Med Genet. 1993. PMID: 8357018

Effect of retinal impulse blockage on cytochrome oxidase-rich zones in the macaque striate cortex: II. Quantitative electron-microscopic (EM) analysis of neuropil.

Wong-Riley MT, Trusk TC, Tripathi SC, Hoppe DA. Wong-Riley MT, et al. Among authors: hoppe da. Vis Neurosci. 1989;2(5):499-514. doi: 10.1017/s0952523800012396. Vis Neurosci. 1989. PMID: 2562110

Effect of retinal impulse blockage on cytochrome oxidase-rich zones in the macaque striate cortex: I. Quantitative electron-microscopic (EM) analysis of neurons.

Wong-Riley MT, Tripathi SC, Trusk TC, Hoppe DA. Wong-Riley MT, et al. Among authors: hoppe da. Vis Neurosci. 1989;2(5):483-97. doi: 10.1017/s0952523800012384. Vis Neurosci. 1989. PMID: 2562109

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