Works matching IS 09646906 AND DT 2003 AND VI 12 AND IP suppl_1
Results: 13
Vascular morphogenesis: tales of two syndromes.
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- Human Molecular Genetics, 2003, v. 12, n. suppl_1, p. R97
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Genetic modifiers in human development and malformation syndromes, including chaperone proteins.
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- Human Molecular Genetics, 2003, v. 12, n. suppl_1, p. R45
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Pathogenesis of split-hand/split-foot malformation.
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- Human Molecular Genetics, 2003, v. 12, n. suppl_1, p. R51, doi. 10.1093/hmg/ddg090
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Lissencephaly and the molecular basis of neuronal migration.
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- Human Molecular Genetics, 2003, v. 12, n. suppl_1, p. R89
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Normal and abnormal dental development.
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- Human Molecular Genetics, 2003, v. 12, n. suppl_1, p. R69
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Roles of BRCA1 in DNA damage repair: a link between development and cancer.
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- Human Molecular Genetics, 2003, v. 12, n. suppl_1, p. R113
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T-box genes in human disorders.
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- Human Molecular Genetics, 2003, v. 12, n. suppl_1, p. R37
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Disorders of cholesterol biosynthesis: prototypic metabolic malformation syndromes.
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- Human Molecular Genetics, 2003, v. 12, n. suppl_1, p. R75
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Beckwith–Wiedemann syndrome demonstrates a role for epigenetic control of normal development.
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- Human Molecular Genetics, 2003, v. 12, n. suppl_1, p. R61
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DNA microarrays and development.
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- Human Molecular Genetics, 2003, v. 12, n. suppl_1, p. R1
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Notch signaling and inherited disease syndromes.
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- Human Molecular Genetics, 2003, v. 12, n. suppl_1, p. R9
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To beat or not to beat: roles of cilia in development and disease.
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- Human Molecular Genetics, 2003, v. 12, n. suppl_1, p. R27
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How a Hedgehog might see holoprosencephaly.
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- Human Molecular Genetics, 2003, v. 12, n. suppl_1, p. R15
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