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Articles: Basic Science/Genetics |
Prior Articles
Turner syndrome phalangeal screening based on a two-stage linear regression concept
Pediatrics International, 08/10/09
Quantitative detection of HCMV-DNA in saliva from infants and breast milk on real-time polymerase chain reaction
Pediatrics International, 08/10/09 No Change in the Age of Diagnosis for Fragile X Syndrome: Findings From a National Parent Survey
Pediatrics, 08/07/09 Haematological disorders in Down syndrome
Paediatrics and Child Health, 08/07/09 Energy intake and energy expenditure among children with polymorphisms of the melanocortin-3 receptor
American Journal of Clinical Nutrition, 08/06/09 Bilateral gonadoblastoma with dysgerminoma and pilocytic astrocytoma with WT1 GT-IVS9 mutation: A 46 XY phenotypic female with Frasier syndrome
Pediatric Blood & Cancer, 08/06/09 Predictors of Virologic Failure and Genotypic Resistance Mutation Patterns in Thai Children Receiving Non-Nucleoside Reverse Transcriptase Inhibitor-Based Antiretroviral Therapy
The Pediatric Infectious Disease Journal, 08/05/09 Development of Visuospatial Ability and Kanji Copying in Williams Syndrome
Pediatric Neurology, 08/05/09 Clinical characteristics of patients with non-specific and non-categorized mitochondrial diseases
Acta Pediatrica, 08/04/09 Epigenetics and Neonatology
NeoReviews, 08/03/09 Congenital diaphragmatic hernia with a pure duplication of chromosome 1q: report of the first surviving case
Pediatric Surgery International, 08/03/09 Refinement of the GINGF3 locus for hereditary gingival fibromatosis
European Journal of Pediatrics, 07/30/09 Cognitive and Neural Development of Individuated Self-Representation in Children
Child Development, 07/29/09 The impact of CD34+ cell dose on platelet engraftment in pediatric patients following unmanipulated haploidentical blood and marrow transplantation
Pediatric Blood & Cancer, 07/29/09 The Relation between Theory of Mind and Executive Functions in Children with Fetal Alcohol Spectrum Disorders
Canadian Journal of Clinical Pharmacology, 07/29/09 Homozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia
Pediatrics International, 07/28/09 Uromodulin mutations causing familial juvenile hyperuricaemic nephropathy lead to protein maturation defects and retention in the endoplasmic reticulum
Human Molecular Genetics, 07/28/09 TSC2/PKD1 Contiguous Gene Syndrome: A Report of 2 Cases With Emphasis on Dermatopathologic Findings
American Journal of Dermatopathology, 07/27/09 Familial small cell carcinoma of the ovary
Pediatric Blood & Cancer, 07/27/09 Muscular Dystrophy: Central Nervous System alpha-Dystroglycan Glycosylation Defects and Brain Malformation
Journal of Child Neurology, 07/27/09
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Indexed Journals: Pediatrics International, Journal of Pediatrics, Current Pediatrics
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250 Available Pages
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