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American Journal of Medical Genetics|December 18, 1998
Centromeric DNA break in a 10;16 reciprocal translocation associated with trisomy 16 confined placental mosaicism and maternal uniparental disomy for chromosome 16J C Wang, P Mamunes, S Y Kou, et al.
Endoscopy International Open|September 3, 2019
Evaluation of a novel low-cost disposable endoscope for visual assessment of the esophagus and stomach in an ex-vivo phantom modelNicolò Garbin, Alexander P Mamunes, Dennis Sohn, et al.
Endoscopy International Open|February 3, 2021
Magnetic flexible endoscope for colonoscopy: an initial learning curve analysisAlexander P Mamunes, Federico Campisano, James Martin, et al.
Clinical Genetics|September 1, 1988
Acid alpha-neuraminidase deficiency: a nephropathic phenotype?K S Roth, J C Chan, N R Ghatak, et al.
American Journal of Human Genetics|May 1, 1978
Phenylketonuria heterozygote detection in families with affected childrenT D Paul, I K Brandt, L J Elsas, et al.
The New England Journal of Medicine|June 10, 1982
Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretionM L Batshaw, S Brusilow, L Waber, et al.
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