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KAL1 wt Allele

Known as: KALIG-1, KMS, HHA 
Human KAL1 wild-type allele is located in the vicinity of Xp22.32 and is approximately 203 kb in length. This allele, which encodes anosmin-1 protein… Expand
National Institutes of Health

Papers overview

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2014
2014
Bone homeostasis is maintained by the balance between bone resorption by osteoclasts and bone formation by osteoblasts… Expand
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Highly Cited
2005
Highly Cited
2005
Kallmann syndrome (KAL) combines hypogonadotropic hypogonadism and anosmia. Hypogonadism is due to Gonadotropin Releasing Hormone… Expand
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2005
2005
We present an analytical solution for the acousto-optical modulation of multiply scattered light in a medium irradiated with a… Expand
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Highly Cited
2001
Highly Cited
2001
OBJECTIVE The association of idiopathic hypogonadotrophic hypogonadism (IHH) with congenital olfactory deficit defines Kallmann's… Expand
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Highly Cited
2001
Highly Cited
2001
Kallmann syndrome (KS) consists of congenital, isolated, idiopathic hypogonadotropic hypogonadism (IHH) and anosmia. The gene… Expand
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Review
1996
Review
1996
A detailed neurological investigation of patients with Kallmann's syndrome (KS) has been performed in an attempt to relate… Expand
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1995
1995
Kallmann's syndrome (KS) is characterised by the association of anosmia and isolated hypogonadotrophic hypogonadism (IHH… Expand
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1994
1994
Kallmann syndrome is an inherited disorder characterized by an abnormality in olfactory system development. The gene for the X… Expand
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Highly Cited
1993
Highly Cited
1993
Kallmann syndrome represents the association of hypogonadotropic hypogonadism with anosmia. Three modes of transmission, X… Expand
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Highly Cited
1989
Highly Cited
1989
Mendelian inherited disorders due to deletions of adjacent genes on a chromosome have been described as "contiguous gene… Expand
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