Investigating the role of X chromosome breakpoints in premature ovarian failure.

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2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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2012年论文

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2012年论文

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name

Investigating the role of X chromosome breakpoints in premature ovarian failure.

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Investigating the role of X chromosome breakpoints in premature ovarian failure.

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Investigating the role of X chromosome breakpoints in premature ovarian failure.

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Investigating the role of X chromosome breakpoints in premature ovarian failure.

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Investigating the role of X chromosome breakpoints in premature ovarian failure.

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Investigating the role of X chromosome breakpoints in premature ovarian failure.

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P1476

Investigating the role of X chromosome breakpoints in premature ovarian failure

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P2093

Antonio Pedicini

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Elena Sala

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Fabiana Saccheri

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Francesca Bertola

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Francesca Crosti

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Leda Dalprà

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Maria Adalgisa Police

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Marialuisa Ventruto

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Nicoletta Villa

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Sara Lissoni

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P2860

X-inactivation profile reveals extensive variability in X-linked gene expression in females

Identification of novel mutations in FOXL2 associated with premature ovarian failure

Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism

Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure

A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility

Biosynthesis of heparan sulphate with diverse structures and functions: two alternatively spliced forms of human heparan sulphate 6-O-sulphotransferase-2 having different expression patterns and properties

A large-scale candidate gene association study of age at menarche and age at natural menopause

Genome-wide association studies identify loci associated with age at menarche and age at natural menopause

Clinical practice. Primary ovarian insufficiency

Mater, a maternal effect gene required for early embryonic development in mice

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1755-8166-5-32

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scholarly article

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10.1186/1755-8166-5-32

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2012-07-16T00:00:00Z

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229089602

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1010550490

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3443441

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