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DIAGNOSIS AND MANAGEMENT OF VARROOSIS IN EUROPEAN HONEY BEES, Apis mellifera L., (HYMENOPTERA: APIDAE) IN AN APIARY.
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- Philippine Journal of Veterinary Medicine, 2020, v. 57, n. 1, p. 118
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- Article
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations.
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- Clinical Genetics, 2019, v. 95, n. 3, p. 420, doi. 10.1111/cge.13493
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- Article
Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly.
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- 2019
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- Publication type:
- journal article
Variable prenatal presentation of Pfeiffer syndrome: Suggested aids to prenatal sonographic diagnosis.
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- 2018
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- Publication type:
- journal article
Bringing state-of-the-art diagnostics to vulnerable populations: The use of a mobile screening unit in active case finding for tuberculosis in Palawan, the Philippines.
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- PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0171310
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- Article
Prognosis of Fetal Parenchymal Cerebral Lesions without Ventriculomegaly in Congenital Toxoplasmosis Infection.
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- 2017
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- journal article
Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway.
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- Human Mutation, 2016, v. 37, n. 12, p. 1329, doi. 10.1002/humu.23038
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- Article
Mutations in the ERCC2 (XPD) gene associated with severe fetal ichthyosis and dysmorphic features.
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- 2016
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- journal article
Fetal anomalies associated with HNF1B mutations: report of 20 autopsy cases.
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- 2016
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- Publication type:
- journal article
Severe X-linked chondrodysplasia punctata in nine new female fetuses.
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- Prenatal Diagnosis, 2015, v. 35, n. 7, p. 675, doi. 10.1002/pd.4591
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- Publication type:
- Article
Outcome of pregnancy following second- or third-trimester intrauterine fetal death.
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- International Journal of Gynecology & Obstetrics, 2014, v. 127, n. 3, p. 275, doi. 10.1016/j.ijgo.2014.06.015
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- Article
Delineation of EFTUD2 Haploinsufficiency-Related Phenotypes Through a Series of 36 Patients.
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- Human Mutation, 2014, v. 35, n. 4, p. 478, doi. 10.1002/humu.22517
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- Article
Prenatal diagnosis of exophytic nevus sebaceous of the scalp.
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- Prenatal Diagnosis, 2013, v. 33, n. 13, p. 1305, doi. 10.1002/pd.4252
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- Article
Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases.
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- Acta Neuropathologica, 2013, v. 126, n. 3, p. 427, doi. 10.1007/s00401-013-1146-1
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- Article
The key role of ultrasound examination in the prenatal diagnosis of epidermolysis bullosa with pyloric atresia.
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- Prenatal Diagnosis, 2013, v. 33, n. 9, p. 908, doi. 10.1002/pd.4137
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- Article
Quantitative assessment of T cell repertoire recovery after hematopoietic stem cell transplantation.
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- Nature Medicine, 2013, v. 19, n. 3, p. 372, doi. 10.1038/nm.3100
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- Article
INFORMATION SEEKING HEURISTICS OF UNDERGRADUATE LIBRARY AND INFORMATION SCIENCE STUDENTS OF THE UNIVERSITY OF THE PHILIPPINES DILIMAN.
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- Journal of Philippine Librarianship, 2013, v. 33, n. 1, p. 15
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- Article
Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies.
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- Brain: A Journal of Neurology, 2012, v. 135, n. 2, p. 469, doi. 10.1093/brain/awr357
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- Article
Prenatal evaluation of the middle ear and diagnosis of middle ear hypoplasia using MRI.
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- Pediatric Radiology, 2011, v. 41, n. 5, p. 652, doi. 10.1007/s00247-010-1913-2
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- Article
High-throughput sequencing of a 4.1 Mb linkage interval reveals FLVCR2 deletions and mutations in lethal cerebral vasculopathy.
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- Human Mutation, 2010, v. 31, n. 10, p. 1134, doi. 10.1002/humu.21329
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- Article
CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation.
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- Human Mutation, 2009, v. 30, n. 11, p. 1574, doi. 10.1002/humu.21116
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- Publication type:
- Article
New Insight on FGFR3-Related Chondrodysplasias Molecular Physiopathology Revealed by Human Chondrocyte Gene Expression Profiling.
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- PLoS ONE, 2009, v. 4, n. 10, p. 1, doi. 10.1371/journal.pone.0007633
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- Article
Retrospective detection of transaldolase deficiency in amniotic fluid: implications for prenatal diagnosis.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 460, doi. 10.1002/pd.2002
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- Publication type:
- Article
Vaginal Delivery Using Cranioclasia following Prenatal Diagnosis of a Giant Fetal Intracranial Teratoma.
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- Fetal Diagnosis & Therapy, 2008, v. 23, n. 3, p. 222, doi. 10.1159/000116745
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- Article
Toxoplasmosis reactivation following HAART introduction associated with foetal death in a severely immune suppressed HIV-infected woman: an immune reconstitution inflammatory syndrome (IRIS) consequence?
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- Retrovirology, 2008, v. 5, p. 1, doi. 10.1186/1742-4690-5-S1-O9
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- Article
Voluminous fetal chylous ascites: a case of complete spontaneous prenatal regression.
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- 2007
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- Publication type:
- journal article
Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis.
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- 2005
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- Publication type:
- Letter
Expression of mutantJAGGED1alleles in patients with Alagille syndrome.
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- Human Genetics, 2005, v. 116, n. 6, p. 445, doi. 10.1007/s00439-005-1262-7
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- Publication type:
- Article
COGNITIVE STYLES AND ACADEMIC PERFORMANCE OF STUDENTS IN LIBRARY AND INFORMATION SCIENCE.
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- Journal of Philippine Librarianship, 2002, v. 23, n. 1/2, p. 1
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- Article
Usefulness of fluorescence in situ hybridization for the diagnosis of Turner mosaic fetuses with small ring X chromosomes.
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- 2000
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- Publication type:
- journal article
Respective role of humoral factors and blood pressure in aortic remodeling of DOCA hypertensive rats.
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- American Journal of Hypertension, 1996, v. 9, n. 10, p. 991, doi. 10.1016/0895-7061(96)00119-7
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- Publication type:
- Article
Respective role of humoral factors and blood pressure in cardiac remodeling of DOCA hypertensive rats.
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- Cardiovascular Research, 1996, v. 31, n. 2, p. 287, doi. 10.1016/0008-6363(95)00201-4
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- Article
Developmental studies demonstrate age-dependent elevation of renin activity in TGR(mRen2)27 rats.
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- American Journal of Hypertension, 1995, v. 8, n. 12, p. 1167, doi. 10.1016/0895-7061(95)00254-5
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- Publication type:
- Article