(Q59287993)

English

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

scientific article published on 01 March 1986

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3007328%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

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 (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3007328%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Kallmann syndrome

1 reference

based on heuristic

inferred from title

X-linked ichthyosis

1 reference

based on heuristic

inferred from title

Andrea Ballabio

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3007328%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

Chiara Mondello

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3007328%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

author name string

G Parenti

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3007328%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

P Tippett

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3007328%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

S Di Maio

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3007328%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

A Tenore

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3007328%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

G Andria

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3007328%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

publication date

1 March 1986

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3007328%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3007328%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

72

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3007328%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3007328%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

237-240

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3007328%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

https://scigraph.springernature.com/pub.10.1007/bf00291885

0 references

The X-linked blood group system Xg. Tests on unrelated people and families of northern European ancestry

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complex glycerol kinase deficiency syndrome explained as X-chromosomal deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ichthyosis vulgaris with hypogenitalism and hypogonadism: evidence for different genotypes by lipoprotein electrophoresis and steroid sulfatase testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X chromosome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on olfactory thresholds in normal man and in patients with adrenal cortical insufficiency: the role of adrenal cortical steroids and of serum sodium concentration

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked syndrome of congenital ichthyosis, hypogonadism, mental retardation and anosmia

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Steroid sulphatase deficiency associated with testis cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Steroid Sulphatase Deficiency is Present in Patients with the Syndrome’ Ichthyosis and Male Hypogonadism’ and with’ Rud Syndrome’

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An RFLP detecting single copy X-chromosome fragment, dic56, from Xp22-Xpter [HGM8 assignment no. DXS 143].

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzymatic basis of typical X-linked icthyosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical spectrum of steroid sulfatase deficiency: X-linked recessive ichthyosis, birth complications and cryptorchidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Steroid sulfatase deficiency and the genetics of the short arm of the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-resolution chromosome analysis in clinical medicine

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Steroid sulphatase deficiency and hypogonadism

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3007328

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00291885

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3007328%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3007328%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

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