Obstetrics / Gynecology /PND
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Caspase 8 deficiency syndrome (sequence analysis of CASP8 gene)
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Caudal regression syndrome (deletion/duplication analysis on VANGL1 gene)
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Caudal regression syndrome (sequence analysis of VANGL1 gene)
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Chromosomal microarray (array CGH, Cytoscan 750K), prenatal test
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Chromosome 14 uniparental disomy (MS-MLPA)
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Chromosome analysis of amniotic fluid
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Chromosome analysis of chorionic villus
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Chromosome analysis of fibroblasts
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Chromosome analysis of stimulated cultures (blood)
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Chromosome analysis of stimulated cultures (fetal blood)
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Chromosome breakage analysis, prenatal
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Ciliopathies (WES based NGS panel for 202 genes)
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Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency (deletion/duplication analysis on CYP17A1 gene)
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Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency (sequence analysis of CYP17A1 gene)
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Congenital dysfibrinogenemia (sequence analysis of FGA gene)
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Congenital dysfibrinogenemia (sequence analysis of FGG gene)
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Craniosynostosis (NGS panel for 5 genes, PND)
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Craniosynostosis (WES based NGS panel of 69 genes)
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Craniosynostosis mutations panel, prenatal
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Culler-Jones syndrome | Holoprosencephaly 9 (sequence analysis of GLI2 gene)
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