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Apr 3, 2024 · A very rare autosomal recessive metabolic disorder (hyperornithinaemia-hyperammonemia-homocitrullinuria syndrome) caused by a deficiency of the mitochondrial ...
Missing: IJAR - | Show results with:IJAR -
Oct 22, 2024 · ... J Med Case Rep. Luma Haj Kassem · Mohamed Fares Ahmado · Majd Sheikh Alganameh. Background: Waardenburg syndrome is a group of rare genetic conditions.
Jan 16, 2024 · ... Indian journal of applied research Volume - 10 |. Issue - 9 | September - 2020 | PRINT ISSN No. 2249 - 555X | DOI: 10.36106/ijar. Physiology. 22. Vinita Ailani.
Dec 28, 2023 · ... applied 1891 applies 1892 apply 1893 applying 1894 appointed 1895 ... case 4680 casein 4681 caseous 4682 caserta 4683 cases 4684 casework 4685 cash ...
Missing: IJAR - | Show results with:IJAR -
Jan 6, 2024 · Treatment for babies with PKU involves supplementing with a phenylalanine-free formula. Formula feedings can be combined with breastfeeding as long as blood ...