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Articles: Basic Science/Genetics |
Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis
European Journal of Pediatrics, 07/02/09
Prior Articles
Sporadic In Utero Generalized Edema Caused by Mutations in the Lymphangiogenic Genes VEGFR3 and FOXC2
The Journal of Pediatrics, 07/01/09 Chromosome Instability in Lymphocytes of Children With Coeliac Disease
Journal of Pediatric Gastroenterology and Nutrition, 07/01/09 Nutri-genetic Determinants of Neural Tube Defects in India
Indian Pediatrics, 06/30/09
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Carbonic Anhydrase II Deficiency: A Novel Mutation
Indian Pediatrics, 06/30/09
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NPHS2 Mutations in Children With Steroid-Resistant Nephrotic Syndrome
Iranian Journal of Kidney Diseases, 06/30/09 Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations
American Journal of Medical Genetics, 06/30/09 Medical Adherence in Young Adolescents with Spina Bifida: Longitudinal Associations with Family Functioning
Journal of Pediatric Psychology, 06/29/09 Analysis of circulating hem-endothelial marker RNA levels in preterm infants
BMC Pediatrics, 06/26/09
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Autism and Hypoplastic Corpus Callosum in a Case of Monocentric Marker Chromosome 15
Pediatric Neurology, 06/26/09 Variant Late Infantile Neuronal Ceroid Lipofuscinosis (CLN6 Gene) in Saudi Arabia
Pediatric Neurology, 06/26/09 Rolandic Mitochondrial Encephalomyelopathy and MT-ND3 Mutations
Pediatric Neurology, 06/26/09 Young Adult Support for Clean Indoor Air Laws in Restaurants and Bars
Journal of Adolescent Health, 06/25/09 Proinflammatory Plasma Cytokines in Children With Migraine
Pediatric Neurology, 06/24/09 Wilms tumor 1 gene mutations are associated with a higher risk of recurrence in young adults with acute myeloid leukemia
Cancer, 06/24/09 The genetic and epigenetic basis of ependymoma
Child's Nervous System, 06/22/09 A heritable cause of cleft lip and palate—Van der Woude syndrome caused by a novel IRF6 mutation. Review of the literature and of the differential diagnosis
European Journal of Pediatrics, 06/22/09 Poland syndrome with bilateral features: Case description with review of the literature
American Journal of Medical Genetics, 06/22/09 Multiple cysts of the corpus callosum and psychomotor delay in a patient with a 3.1 Mb 15q24.1q24.2 interstitial deletion identified by array-CGH
American Journal of Medical Genetics, 06/22/09 Congenital bilateral amazia associated with bilateral choanal atresia
American Journal of Medical Genetics, 06/22/09
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Indexed Journals: Pediatrics International, Journal of Pediatrics, Current Pediatrics
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