Clinical, Biochemical, and Molecular Characteristics of Filipino Patients with Tyrosinemia Type 1 von 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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PMD patient mutations reveal a long-distance intronic interaction that regulates PLP1/DM20 alternative splicing von Taube, Jennifer R, Sperle, Karen, Banser, Linda, Seeman, Pavel, Cavan, Barbra Charina V, Garbern, James Y, Hobson, Grace M

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AB059. The clinical profile and factors influencing loss to follow-up on the use of repeat otoacoustic emissions (OAE) and auditory brainstem response (ABR) among infants with refe... von Dominguez, Ana Noelle M., Cavan, Barbra Charina V.

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Osteogenesis Imperfecta Type V: A Report of Two Filipino Families and Review of Literature von Baluyot, Melissa Mae P., Cavan, Barbra Charina V., Alcausin, Maria Melanie Liberty B.

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Volunteer Youth Leaders for Health - Philippines: Providing a Mechanism for Youth Empowerment towards Advocacy for Birth Defects Prevention and Care von Padilla, Carmencita D., Sur, Aster Lynn D., Pascual, Ryan John P., Enriquez, Christian Emmanuel P., Adducul, Rufus Thomas Y., Tumulak, Ma-Am Joy R., De la Paz, Eva Maria C., Berboso, April Grace D., Abarquez, Conchita G., Dizon, Florencio C.

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A Case of Spinal Muscular Atrophy Type 1 in a Filipino Infant von Cavan, Barbra Charina V., Reroma, Aubrey E., Modequillo, Margaret S.

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Establishment of the Philippine Birth Defects Surveillance von David-Padilla, Carmencita, Cutiongco-de la Paz, Eva Maria, Cavan, Barbra Charina V., Abarquez, Conchita G., Sur, Aster Lynn D., Sales, Rommel I., Posecion, Edgar Winston C., Orbillo, Lita L., Basilio, Juanita A.

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Intravenous Pamidronate Treatment in Filipino Children with Moderate to Severe Osteogenesis Imperfecta von Alcausin, Maria Melanie B., De Dios, John Karl L., Chiong, Mary Anne D., Cavan, Barbra Charina V., David-Padilla, Carmencita

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Complete Sternal Cleft in a Filipino Newborn von Cavan, Barbra Charina V., Masongsong, Jonna A., Mancao, Peter Y., Tan, Arnold A.

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Thrombocytopenia in a Filipino Child with Mosaic Monosomy 21/ Ring Chromosome 21 von Cavan, Barbra Charina V., Serafica, Edgardo Martin C., Modequillo, Margaret S., Melicor, Cynthia F.

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A Filipino Child with Dyskeratosis Congenita with a C→T substitution on nucleotide 1058 of the DKC1 gene von Bas-Bucao, Miraflor, Cavan, Barbra Charina V., Limchiu, Susana Deborah P., Metzenberg, Aida

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Ellis-van Creveld Syndrome in Two Filipino Siblings von Cavan, Barbra Charina V., Amatong, Rudy A., Serafica, Edgardo Martin C., Cavan-Jumamoy, Bridget Christa V., Jiao III, Leopoldo L.

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