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1. Phenotypic expression of the fibroblast growth factor receptor 3 (FGFR3) mutation P250R in a large craniosynostosis family.


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2. Phenotypic expression of the fibroblast growth factor receptor 3 (FGFR3) mutation P250R in a large craniosynostosis family.

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3. De novo deletion (14)(q11.2q13) including PAX9: clinical and molecular findings

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4. Mosaicism for a dup(12)(q22q13) in a patient with hypomelanosis of Ito and asymmetry

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1757152
http://www.ncbi.nlm.nih.gov/pubmed/11183189  
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5. Miniature tensile and shear creep experiments for the characterization of gas turbine blade materials


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6. Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232.

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7. Multiplex-FISH for pre- and postnatal diagnostic applications.

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8. Direct assessment of the creep strength of DS cast turbine blades using miniature creep specimens


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9. Molecular modelling of the norrie disease protein predicts a cystine knot growth factor tertiary structure


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10. Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogenetics


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