Skip to search formSkip to main contentSkip to account menu

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… 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2005
Highly Cited
2005
Kallmann syndrome (KAL) combines hypogonadotropic hypogonadism and anosmia. Hypogonadism is due to Gonadotropin Releasing Hormone… 
Highly Cited
2005
Highly Cited
2005
We present an analytical solution for the acousto-optical modulation of multiply scattered light in a medium irradiated with a… 
Review
2003
Review
2003
Congenital abnormalities of the kidney and urinary tract, CAKUT are common in humans, occurring at a frequency of approximately 1… 
Highly Cited
2001
Highly Cited
2001
OBJECTIVE The association of idiopathic hypogonadotrophic hypogonadism (IHH) with congenital olfactory deficit defines Kallmann's… 
Highly Cited
2001
Highly Cited
2001
Kallmann syndrome (KS) consists of congenital, isolated, idiopathic hypogonadotropic hypogonadism (IHH) and anosmia. The gene… 
Review
1996
Review
1996
A detailed neurological investigation of patients with Kallmann's syndrome (KS) has been performed in an attempt to relate… 
Highly Cited
1994
Highly Cited
1994
Kallmann syndrome is an inherited disorder characterized by an abnormality in olfactory system development. The gene for the X… 
Highly Cited
1993
Highly Cited
1993
Kallmann syndrome represents the association of hypogonadotropic hypogonadism with anosmia. Three modes of transmission, X… 
Highly Cited
1989
Highly Cited
1989
Mendelian inherited disorders due to deletions of adjacent genes on a chromosome have been described as "contiguous gene…