18 results on '"Dahl, N."'
Search Results
2. Clinical diagnostics of autosomal dominant aplasia of lacrimal and salivary glands (ALSG) associated with mutations in the fibroblast growth factor 10 gene: OS058
3. Re-evaluation of the dysequilibrium syndrome
4. Central nervous system involvement in severe congenital neutropenia: neurological and neuropsychological abnormalities associated with specific HAX1 mutations
5. INTRAVITREAL TRIAMCINOLONE ACETONIDE AND BEVACIZUMAB IN DIABETIC MACULAR EDEMA TREATMENT
6. Effects of oxybutynin transdermal system on health-related quality of life and safety in men with overactive bladder and prostate conditions
7. Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis
8. Hemizygosity for chromosome 2q14.2-q22.1 spanning the GLI2 and PROC genes associated with growth hormone deficiency, polydactyly, deep vein thrombosis and urogenital abnormalities
9. VALIDATION OF THE WORK PRODUCTIVITY QUESTIONNAIRE: RESULTS OF THE MATRIX STUDY: PR6
10. Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGH
11. Clinical diagnostics of autosomal dominant aplasia of lacrimal and salivary glands (ALSG) associated with mutations in the fibroblast growth factor 10 gene: OS058
12. Assignment of the locus for ichthyosis prematurity syndrome to chromosome 9q33.3–34.13
13. Rapp-Hodgkin and AEC syndromes due to a new frameshift mutation in the TP63 gene
14. Depression in relation to age and gender in the general population: the Nord-Trøndelag Health Study (HUNT)
15. CENTRAL MODULATION OF EXERCISE-INDUCED MUSCLE PAIN
16. INTERACTION BETWEEN MUSCLE TEMPERATURE AND BLOOD FLOW ON MUSCLE SYMPATHETIC OUTFLOW DURING FOREARM EXERCISE
17. A microdeletion syndrome due to a 3-Mb deletion on 19q13.2 - Diamond-Blackfan anemia associated with macrocephaly, hypotonia, and psychomotor retardation
18. Diamond-Blackfan anaemia in the Italian population
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