Obstetrics / Gynecology /PND
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Hereditary endocrinopathies in infertility (sequence analysis of CYP21A2, SRD5A2, CYP19A1, ESR1, ESR2, AR genes and deletion/duplication analysis of CYP21A2 gene)
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Hereditary thrombophilia due to congenital antithrombin deficiency, c.41+141G>A polimorphism on SERPINC1 gene
+ info
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Holoprosencephaly (deletion/duplication analysis on PTCH, SHH, ZIC2, SIX3, TGIF, TRAPPC10, GLI2 and FBXW11 genes)
+ info
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Holoprosencephaly (deletion/duplication analysis on SHH gene)
+ info
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Holoprosencephaly (NGS panel of 9 genes)
+ info
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Holoprosencephaly (sequence analysis of SHH gene)
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Holoprosencephaly (sequence analysis of ZIC2 gene)
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Holoprosencephaly 11 (sequence analysis of CDON gene)
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Holoprosencephaly 2 (sequence analysis of SIX3 gene)
+ info
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Holoprosencephaly 4 (sequence analysis of TGIF1 gene)
+ info
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Hydatidiform mole (sequence analysis of NLRP7 gene)
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Hydatidiform mole, recurrent 2 (sequence analysis of KHDC3L gene)
+ info
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Hydrocephalus, X-linked (deletion/duplication analysis of L1CAM gene)
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Hydrocephalus, X-linked (sequence analysis of L1CAM gene)
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Hydrolethalus syndrome (sequence analysis of HYLS1 gene)
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Hypogonadism, hypogonadotropic (sequence analysis of LHB gene)
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Hypogonadotropic hypogonadism (NGS panel of 26 genes)
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Hypogonadotropic hypogonadism 11 with or without anosmia (sequence analysis of TACR3 gene)
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Hypogonadotropic hypogonadism 12 with or without anosmia (sequence analysis of GNRH1 gene)
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Hypogonadotropic hypogonadism 13 with or without anosmia (sequence analysis of KISS1 gene)
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