<![CDATA[Department of Health Elibrary Search for 'au:"Chiong, Mary Anne D. "']]>

<![CDATA[Department of Health Elibrary Search for 'au:"Chiong, Mary Anne D. "']]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-search.pl?q=ccl=au%3A%22Chiong%2C%20Mary%20Anne%20D.%20%22&sort_by=relevance&format=rss 21 0 50 Etiology of congenital hypothyroidism among infants screen by the Philippine newborn screening program / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2742

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2742 Profile of Filipino infants with 21-hydroxylase deficiency congenital adrenal hyperplasia detected by the Philippine newborn screening program / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2939

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2939 Characterization of mutations at nucleotide 1138 of the fibroblast growth factor receptor 3 gene in Filipino patients with achondroplasia / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2965

]]> Place hold on Characterization of mutations at nucleotide 1138 of the fibroblast growth factor receptor 3 gene in Filipino patients with achondroplasia /

]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2965 Correlation between dried blood spot thin layer chromatography and plasma high performance liquid chromatography of leucine/isoleucine levels among Filipino patients with maple syrup urine disease (MSUD) seen at the Institute of Human Genetics, National Institutes of Health / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2966

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2966 Gaucher disease in six Filipino children: a case series / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2972

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2972 Oto-palatodigital syndrome in a Filipino child / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2973

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2973 Malignant infantile osteopetrosis in a Filipino child / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2974

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2974 Trisomy 8 mosaicism in Two Filipino children / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2976

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2976 Multiple congenital anomalies in a Filipino infant with trisomy X syndrom / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2977

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2977 Ring chromosome 13 in a Filipino child– a new category with new features? / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2978

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2978 Methylmalonic acidemia in two Filipino children / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2979

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2979 A review of the results of chromosomal analyses done at the National Institutes of Health from 1991 to 2007 / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3005

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3005 Translocation down syndrome among Filipinos and its implications on genetic counseling / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3006

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3006 Molecular analysis of the MUT gene in Filipino patients with methylmalonic acidemia / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3009

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3009 Enzyme replacement therapy in Filipino patients with Gaucher disease and Pompe disease / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3010

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3010 X-linked adrenoleukodystrophy in three Filipino families / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3012

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3012 Misoprostol teratogenicity in six Filipino children : ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3014

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3014 Etiology of congenital hypothyroidism among infants screen by the Philippine newborn screening program / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3016

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3016 Galactosemia in three Filipino patients - The importance of newborn screening / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3111

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3111 Two Filipino patients with 6-pyruvoyltetrahydropterin synthase deficiency / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3112

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3112 Mutations of the phenylalanine hydroxylase (PAH) gene in Filipino patients with phenylketonuria / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3118

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3118