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Articles: Basic Science/Genetics



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Prior Articles


Turner syndrome phalangeal screening based on a two-stage linear regression concept
Pediatrics International, 08/10/09
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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 more...
250 Available Pages
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