Children's Hospital Central California View Homepage


Ontology type: grid:Healthcare  | foaf:Organization     


Organization Info

Publications in SciGraph latest 20 shown

  • 2019-12 Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language in NATURE COMMUNICATIONS
  • 2019-03-14 Recurrent KBTBD4 small in-frame insertions and absence of DROSHA deletion or DICER1 mutation differentiate pineal parenchymal tumor of intermediate differentiation (PPTID) from pineoblastoma in ACTA NEUROPATHOLOGICA
  • 2019-01 The genetic landscape of gliomas arising after therapeutic radiation in ACTA NEUROPATHOLOGICA
  • 2018-12 The genetic landscape of ganglioglioma in ACTA NEUROPATHOLOGICA COMMUNICATIONS
  • 2018-12 Group B streptococcal colonization in mothers and infants in western China: prevalences and risk factors in BMC INFECTIOUS DISEASES
  • 2018-12 CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language in NATURE COMMUNICATIONS
  • 2018-12 Epidemiology of birth defects based on surveillance data from 2011–2015 in Guangxi, China: comparison across five major ethnic groups in BMC PUBLIC HEALTH
  • 2018-08 Identifying and Addressing Genetic Counseling Challenges among Indigenous People of Oaxaca—One Center’s Experience with Two Immigrant Farmworker Families in the Central Valley of California in JOURNAL OF GENETIC COUNSELING
  • 2018-04 Deep sequencing of WNT-activated medulloblastomas reveals secondary SHH pathway activation in ACTA NEUROPATHOLOGICA
  • 2017-01 Survival after chemotherapy and stem cell transplant followed by delayed craniospinal irradiation is comparable to upfront craniospinal irradiation in pediatric embryonal brain tumor patients in JOURNAL OF NEURO-ONCOLOGY
  • 2016-07 IDH1 mutation can be present in diffuse astrocytomas and giant cell glioblastomas of young children under 10 years of age in ACTA NEUROPATHOLOGICA
  • 2016-01 De novo missense variants in PPP2R5D are associated with intellectual disability, macrocephaly, hypotonia, and autism in NEUROGENETICS
  • 2016-01 The Extended Clinical Phenotype of 26 Patients with Chronic Mucocutaneous Candidiasis due to Gain-of-Function Mutations in STAT1 in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2015-09 Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1 in JOURNAL OF NEUROLOGY
  • 2015-05 Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utility in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-04 Association of genetic variation in IKZF1, ARID5B, and CEBPE and surrogates for early-life infections with the risk of acute lymphoblastic leukemia in Hispanic children in CANCER CAUSES & CONTROL
  • 2015-01 Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy in NATURE GENETICS
  • 2014-11 Incidence and associated factors of difficult tracheal intubations in pediatric ICUs: a report from National Emergency Airway Registry for Children: NEAR4KIDS in INTENSIVE CARE MEDICINE
  • 2014-10 Device Closure of Secundum Atrial Septal Defects in Infants Weighing Less Than 8 Kg in PEDIATRIC CARDIOLOGY
  • 2014-08 Assessing the impact of short-term surgical education on practice: a retrospective study of the introduction of mesh for inguinal hernia repair in sub-Saharan Africa in HERNIA
  • JSON-LD is the canonical representation for SciGraph data.

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    Download the RDF metadata as:  json-ld nt turtle xml License info

    HOW TO GET THIS DATA PROGRAMMATICALLY:

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    RDF/XML is a standard XML format for linked data.

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    This table displays all metadata directly associated to this object as RDF triples.

    60 TRIPLES      13 PREDICATES      14 URIs      6 LITERALS

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