Clinical, Biochemical, and Molecular Characteristics of Filipino Patients with Tyrosinemia Type 1 by Cavan, Barbra Charina V, de Castro-Hamoy, Leniza G, Abarquez, Conchita G, Maceda, Ebner Bon G, Alcausin, Maria Melanie Liberty B

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Integrating Genetic Services in the Philippine Public Health Delivery System: The Value of Networks by Padilla, Carmencita D, Abadingo, Michelle E, Maceda, Ebner Bon G, Alcausin, Maria Melanie Liberty B

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Newborn Screening Long-Term Follow-Up Clinics (Continuity Clinics) in the Philippines during the COVID-19 Pandemic: Continuing Quality Patient Care by Maceda, Ebner Bon G, Abadingo, Michelle E, Panol, Karen Asuncion R, Beltran, Frederick David E, Valdez-Acosta, Ivy Rose C, Taquiqui, Grandelee D, Gawigawen, Sharon B, Macalino, Maria Victoria L, Aguirre-Aguinaldo, Laura Maria Soledad M, Flores-Declaro, Marive A, Ventilacion, Karen June V, Boligao, Ma Rita Anna Salve R, Honor, Nancy G, Ellong, Mirasol S, Ocho-Ortencio, Rona D, Beley, Genelynne J, Bondoc-Eran, Maria Christina N, Therrell, Jr, Bradford L, Padilla, Carmencita D

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The clinical utility of polygenic risk scores in genomic medicine practices: a systematic review by Kumuthini, Judit, Zick, Brittany, Balasopoulou, Angeliki, Chalikiopoulou, Constantina, Dandara, Collet, El-Kamah, Ghada, Findley, Laura, Katsila, Theodora, Li, Rongling, Maceda, Ebner Bon, Monye, Henrietta, Rada, Gabriel, Thong, Meow-Keong, Wanigasekera, Thilina, Kennel, Hannah, Marimuthu, Veeramani, Williams, Marc S., Al-Mulla, Fahd, Abramowicz, Marc

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Successful Implementation of Newborn Screening for Hemoglobin Disorders in the Philippines by Padilla, Carmencita D, Therrell, Jr, Bradford L, Alcausin, Maria Melanie Liberty B, de Castro, Jr, Reynaldo C, Gepte, Maria Beatriz P, Reyes, Ma Elouisa L, Jomento, Charity M, Suarez, Riza Concordia N, Maceda, Ebner Bon G, Abarquez, Conchita G, Posecion, J Edgar Winston C, Andal, Alma P, Elizaga, Anna Lea G, Halili-Mendoza, Bernadette C, Otayza, Maria Paz Virginia K, Hoppe, Carolyn C

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Philippine Performance Evaluation and Assessment Scheme (PPEAS): Experiences in Newborn Screening System Quality Improvement by Padilla, Carmencita D, Therrell, Bradford L, Panol, Karen Asuncion R, Suarez, Riza Concordia N, Reyes, Ma Elouisa L, Jomento, Charity M, Maceda, Ebner Bon G, Lising, Jovy Ann C, Beltran, Frederick David E, Orbillo, Lita L

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Maple syrup urine disease associated with nephrotic syndrome in a Filipino child by Maceda, Ebner Bon G, Abadingo, Michelle E, Magbanua-Calalo, Cheryll J, Dator, Melissa A, Resontoc, Lourdes Paula R, Castro-Hamoy, Leniza De, Abacan, Mary Ann R, Chiong, Mary Anne D, Estrada, Sylvia C

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Acceptability of dried blood spot collection by primary caregivers of Filipino patients with maple syrup urine disease (MSUD) and phenylketonuria (PKU) by Merencilla, Roxanne Janica E., Maceda, Ebner Bon G., Basas, Jeanne Ruth U., Adducul, Rufus Thomas Y., Francisco, Ma. Lourdes, Licudo, Justin Von, de Castro-Hamoy, Leniza G.

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Acceptance, Knowledge, and Experiences of Pediatric Hematologists in the Philippines on Newborn Screening for Hemoglobinopathies by de Castro, Reynaldo C., Maceda, Ebner Bon G., Alcausin, Maria Melanie Liberty B.

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Telegenetics Services in a Tertiary Hospital: Utility and Patient Satisfaction by Herlao, Irish Alysa V., Maceda, Ebner Bon G., Abacan, Mary Ann R., de Castro-Hamoy, Leniza G., Alcausin, Maria Melanie Liberty B.

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Novel NSDHL gene variant for congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD) syndrome by Maceda, Ebner Bon Gatus, Kratz, Lisa E, Ramos, Veronica Marie E, Abacan, Mary Ann R

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