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English
The gene for X-linked Kallmann syndrome: a human neuronal migration defect.
scientific article published on June 1992
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504616
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504616%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
review article
1 reference
stated in
Europe PubMed Central
title
The gene for X-linked Kallmann syndrome: a human neuronal migration defect
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504616
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504616%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
main subject
Kallmann syndrome
1 reference
based on heuristic
inferred from title
author
Andrea Ballabio
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504616
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504616%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
author name string
G Camerino
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504616
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504616%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
language of work or name
English
1 reference
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publication date
1 June 1992
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504616
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504616%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
published in
Current Opinion in Genetics & Development
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504616
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504616%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
volume
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504616
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504616%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504616
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504616%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
page(s)
417-421
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504616
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504616%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
cites work
Effect of Purified Luteinizing Hormone Releasing Factor on Normal and Hypogonadotrophic Anosmic Men
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Magnetic resonance imaging of the brain in patients with anosmia and hypothalamic hypogonadism (Kallmann's syndrome).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
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inferred from DOI database lookup
The syndrome of anosmia with hypogonadotropic hypogonadism: a genetic study of 18 new families and a review
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new syndrome of anosmia, ichthyosis, hypogonadism, and various neurological manifestations with deficiency of steroid sulfatase and arylsulfatase C
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cortically evoked motor responses in patients with Xp22.3-linked Kallmann's syndrome and in female gene carriers.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Origin of luteinizing hormone-releasing hormone neurons
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heterogeneity of Kallmann's syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Contiguous gene syndromes: a component of recognizable syndromes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Male infant with ichthyosis, Kallmann syndrome, chondrodysplasia punctata, and an Xp chromosome deletion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two cases of steroid sulfatase deficiency with complex phenotype due to contiguous gene deletions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Long-range physical mapping around the human steroid sulfatase locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two families of low-copy-number repeats are interspersed on Xp22.3: Implications for the high frequency of deletions in this region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The WDNM1 gene product is a novel member of the 'four-disulphide core' family of proteins.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
The cell adhesion molecule Cell-CAM 105 is an ecto-ATPase and a member of the immunoglobulin superfamily
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Contact and adhesive specificities in the associations, migrations, and targeting of cells and axons
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic analysis of a Drosophila neural cell adhesion molecule: interaction of fasciclin I and Abelson tyrosine kinase mutations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Interaction of bride of sevenless membrane-bound ligand and the sevenless tyrosine-kinase receptor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Non-inactivation of an X-Chromosome Locus in Man
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Differential expression of steroid sulphatase locus on active and inactive human X chromosome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: evidence for an inversion of the Y chromosome during primate evolution
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linkage of steroid sulphatase in the mouse is evidence for a functional Y-linked allele
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980152-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0959-437X(05)80152-2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504616
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504616%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
PubMed publication ID
1504616
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504616
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504616%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
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