The gene for X-linked Kallmann syndrome: a human neuronal migration defect. (Q35716481)

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20 September 2019

review article

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title

The gene for X-linked Kallmann syndrome: a human neuronal migration defect (English)

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20 September 2019

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1

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20 September 2019

author name string

G Camerino

series ordinal

2

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20 September 2019

language of work or name

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1 June 1992

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Current Opinion in Genetics & Development

20 September 2019

published in

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20 September 2019

volume

2

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20 September 2019

issue

3

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20 September 2019

page(s)

417-421

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Effect of Purified Luteinizing Hormone Releasing Factor on Normal and Hypogonadotrophic Anosmic Men

20 September 2019

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Magnetic resonance imaging of the brain in patients with anosmia and hypothalamic hypogonadism (Kallmann's syndrome).

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A new syndrome of anosmia, ichthyosis, hypogonadism, and various neurological manifestations with deficiency of steroid sulfatase and arylsulfatase C

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Origin of luteinizing hormone-releasing hormone neurons

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Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome

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Heterogeneity of Kallmann's syndrome

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X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosome

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Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndrome

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Male infant with ichthyosis, Kallmann syndrome, chondrodysplasia punctata, and an Xp chromosome deletion

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Two cases of steroid sulfatase deficiency with complex phenotype due to contiguous gene deletions

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Long-range physical mapping around the human steroid sulfatase locus

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Two families of low-copy-number repeats are interspersed on Xp22.3: Implications for the high frequency of deletions in this region

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The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

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7 January 2021

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

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7 January 2021

Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome

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7 January 2021

The WDNM1 gene product is a novel member of the 'four-disulphide core' family of proteins.

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The cell adhesion molecule Cell-CAM 105 is an ecto-ATPase and a member of the immunoglobulin superfamily

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Contact and adhesive specificities in the associations, migrations, and targeting of cells and axons

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Genetic analysis of a Drosophila neural cell adhesion molecule: interaction of fasciclin I and Abelson tyrosine kinase mutations.

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Interaction of bride of sevenless membrane-bound ligand and the sevenless tyrosine-kinase receptor

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Non-inactivation of an X-Chromosome Locus in Man

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7 January 2021

Differential expression of steroid sulphatase locus on active and inactive human X chromosome

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7 January 2021

The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: evidence for an inversion of the Y chromosome during primate evolution

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A deletion map of the human Yq11 region: Implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis

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X-linkage of steroid sulphatase in the mouse is evidence for a functional Y-linked allele

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7 January 2021

10.1016/S0959-437X(05)80152-2

Identifiers

DOI

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20 September 2019

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