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Genotype-Phenotype Correlation in Eight New Patients With a Deletion Encompassing 2q31.1
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PORCN Mutations in Focal Dermal Hypoplasia: Coping with Lethality (vol 30, pg E618, 2009)
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Improved Detection of Chromosomal Abnormalities in Chronic Lymphocytic Leukemia by Conventional Cytogenetics Using CpG Oligonucleotide and Interleukin-2 Stimulation: A Belgian Multicentric Study
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Quantitation of Replication of the HCV Genome in Human Livers With End-Stage Cirrhosis by Strand-Specific Real-Time RT-PCR Assays: Methods and Clinical Relevance
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On the Adjustment for Covariates in Genetic Association Analysis: A Novel, Simple Principle to Infer Direct Causal Effects
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High-resolution analysis of plantar pressure in habitually shod and unshod humans
(2009) p.114-115 -
Attentional load modifies early activity in human primary visual cortex
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Mesomelic Dysplasia With Acral Synostoses Verloes-David-Pfeiffer Type: Follow-Up Study Documents Progressive Clinical Course
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Hartsfield Holoprosencephaly-Ectrodactyly Syndrome in Five Male Patients: Further Delineation and Review
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CLINICAL PHARMACY ACTIVITIES AT A PEDIATRIC HEMATO-ONCOLOGY UNIT