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Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability
by
Park, Woo-Jin
,
Meyers, Gregory A.
,
Li, Xiang
,
Theda, Christiane
,
Day, Donald
,
Oriow, Seth J.
,
Jones, Marilyn C.
,
Jabs, Ethylin Wang
Published in
Human molecular genetics
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Hum Mol Genet
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Human Molecular Genetics
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Alleles
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Amino Acid Sequence
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Base Sequence
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Biochemistry & Molecular Biology
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Biological And Medical Sciences
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Craniofacial Dysostosis - Epidemiology
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Craniofacial Dysostosis - Genetics
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Craniosynostoses - Complications
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Craniosynostoses - Epidemiology
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Craniosynostoses - Genetics
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Craniosynostosis
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Crouzon's Syndrome
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Diseases Of The Osteoarticular System
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Exons
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Female
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Fgfr2 Gene
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Fibroblast Growth Factor Receptors
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Genetic Heterogeneity
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Genetic Variation
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Genetics & Heredity
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