 | Articles: Basic Science/Genetics |
Prenatal diagnosis of triple X using fetal cells obtained by endocervical lavage
Prenatal Diagnosis, 05/30/03
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Mitochondrial dysfunction in autistic patients with 15q inverted duplication
Annals of Neurology , 05/29/03
Hypoparathyroidism and 22q11 deletion syndrome
BMJ - Archives of Diseases in Childhood, 05/27/03
22q11 deletion: a multisystem disorder requiring multidisciplinary input
BMJ - Archives of Diseases in Childhood, 05/27/03
Effect of genotype on phenotype and mortality in cystic fibrosis: a retrospective cohort study
The Lancet, 05/22/03
Outcome and survival of 88 patients with urea cycle disorders: a retrospective evaluation
European Journal of Pediatrics, 05/20/03
Matrix metalloproteinases and their tissue inhibitors in severely burned children
Wound Repair and Regeneration, 05/19/03
Rapidly progressive adenomatous polyposis in a patient with germline mutations in both the APC and MLH1 genes: the worst of two worlds
Gut, 05/12/03
Profilin is required for viral morphogenesis, syncytium formation, and cell-specific stress fiber induction by respiratory syncytial virus
BMC Infectious Diseases, 05/12/03
Factor V leiden and prothrombin gene G20210A mutation in children with cerebral thromboembolism
American Journal of Hematology, 05/12/03
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Indexed Journals: Pediatrics International, Journal of Pediatrics, Current Pediatrics
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221 Available Pages
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