Paper · 7017147

Localisation of male determining factors in man: a thorough review of structural anomalies of the Y chromosome.

Davis RM. J Med Genet, 1981. Cited by 141 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

Cite this record

ConductScience Library. Localisation of male determining factors in man: a thorough review of structural anomalies of the Y chromosome. Papers, record 7017147. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/7017147

On this page

Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title: Localisation of male determining factors in man: a thorough review of structural anomalies of the Y chromosome.; PubMed
Journal: J Med Genet; PubMed
Year: 1981; PubMed
Publication types: Journal Article, Review; PubMed
PubMed: https://pubmed.ncbi.nlm.nih.gov/7017147/; PubMed
DOI: https://doi.org/10.1136/jmg.18.3.161; PubMed
PMC: https://pmc.ncbi.nlm.nih.gov/articles/PMC1048703/; PubMed
The journal: https://conductscience.org/library/journal-index/2985087R; PubMed
Citations, by iCite: 141; iCite
Relative citation ratio, by iCite: 4.69; iCite
Revised in PubMed: 2019-05-03; PubMed

Authors1

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

Order	Author	Forename	Kind	ORCID iD
1	Davis RM	R M

Source PubMed

Topics20

NLM's MeSH indexing of the paper, its major topics first.

MeSH term	Major
Sex Chromosome Aberrations	Major topic
Sex Chromosomes	Major topic
Sex Determination Analysis	Major topic
Y Chromosome	Major topic
Adolescent
Adult
Aged
Child
Child, Preschool
Female
Humans
Infant
Infant, Newborn
Infertility, Male
Karyotyping
Male
Middle Aged
Oligospermia
Testis
Turner Syndrome

Source PubMed

Grants0

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

None in this release.

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References273

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

Order	PMID	Title	Journal	Year	In Papers	Source
1	7,188,927	Structural abnormalities of the Y chromosome and abnormal external genitals.	Hum Genet	1980	https://conductscience.org/library/papers/7188927	PubMed
2	4,134,689	Letter: Possible evidence for Xp plus in and XX Male.	Lancet	1974	https://conductscience.org/library/papers/4134689	PubMed
3	5,525,760	Structural exchange between the X and Y chromosomes as the probable cause of hypogonadism.	Hereditas	1970	https://conductscience.org/library/papers/5525760	PubMed
4	4,768,114	Renovascular hypertension. Prospective diagnostic yield in a random access population.	Humangenetik	1973	https://conductscience.org/library/papers/4768114	PubMed
5	4,763,930	Pericentric Y inversion in the general population.	Humangenetik	1973	https://conductscience.org/library/papers/4763930	PubMed
6	468,260	Increased HK1 activity levels in the red cells of a patient with a de novo trisomy 10p: t(Y;10)(p11;p12).	Hum Genet	1979	https://conductscience.org/library/papers/468260	PubMed
7	65,650	Possible evidence of X-Y interchange in an XX male.	Lancet	1977	https://conductscience.org/library/papers/65650	PubMed
8	4,261,167	Structural variation in human nitotic chromosomes.	Ann Acad Sci Fenn Biol	1971	https://conductscience.org/library/papers/4261167	PubMed
9	4,109,473	Pitfalls in prenatal diagnosis resulting from chromosomal mosaicism.	J Pediatr	1972	https://conductscience.org/library/papers/4109473	PubMed
10	1,261,075	45,XO/46,XYg dic mosaicism in a patient with ambiguous genitalia.	Clin Genet	1976	https://conductscience.org/library/papers/1261075	PubMed

1 to 10 of 273

See all 273 references

Cited by39

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 141 citations.

PMID	Title	Journal	Year	In Papers	Source
27,355,317	A Track Record on SHOX: From Basic Research to Complex Models and Therapy.	Endocr Rev	2016	https://conductscience.org/library/papers/27355317	PubMed
24,496,683	Clinical characteristics, cytogenetic and molecular findings in patients with disorders of sex development.	J Huazhong Univ Sci Technolog Med Sci	2014	https://conductscience.org/library/papers/24496683	PubMed
11,134,233	SHOX haploinsufficiency and overdosage: impact of gonadal function status.	J Med Genet	2001	https://conductscience.org/library/papers/11134233	PubMed
9,497,950	Male pseudohermaphroditism due to 5 alpha-reductase-2 deficiency in an Arab kindred.	Postgrad Med J	1997	https://conductscience.org/library/papers/9497950	PubMed
7,789,944	Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features.	Hum Genet	1995	https://conductscience.org/library/papers/7789944	PubMed
7,516,747	Y353/B: a candidate multiple-copy spermiogenesis gene on the mouse Y chromosome.	Mamm Genome	1994	https://conductscience.org/library/papers/7516747	PubMed
6,892,019	Translocation(X;Y)(p22.33;p11.2) in XX males: etiology of male phenotype.	Hum Genet	1982	https://conductscience.org/library/papers/6892019	PubMed
6,885,076	A deletion of heterochromatin only of the Y chromosome in an azoospermic male.	Hum Genet	1983	https://conductscience.org/library/papers/6885076	PubMed
6,866,124	Genetics. Sex is simple.	Nature	1983	https://conductscience.org/library/papers/6866124	PubMed
6,745,929	Satellited Y chromosomes: structure, origin, and clinical significance.	Hum Genet	1984	https://conductscience.org/library/papers/6745929	PubMed

1 to 10 of 39

See all 39 cited by

Genes1

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

Gene	NCBI Gene ID	Linked by	In Genes
SRY	6,736	PubTator's text mining	https://conductscience.org/library/genes/6736

Source NCBI Gene

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed: 2026-11-06; PubMed
iCite: 2026-11-05; iCite
PMC's ID file: 2026-11-05; PMC's ID file
NIH RePORTER's grant and paper links: 2026-11-01; NIH RePORTER's grant and paper links
Trials: 2026-11-12
Gene search: 2026-11-11
Pipelines: 2026-09-18

Sources 11

ChEMBL, through Open TargetsCC BY-SA 3.0
ClinicalTrials.govNo license stated
HGNCCC0
iCiteCC BY 4.0
NCBI GenePublic domain (US government)
NIH RePORTER's grant and paper linksPublic domain
Open TargetsCC0 1.0
PMC's ID filePublic domain (US government)
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0

Each source's terms

ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
ClinicalTrials.govnone stated
HGNCCC0: https://www.genenames.org/about/license/
iCiteCC BY 4.0
NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this paper from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/papers/v1/7017147

GET https://conductscience.org/api/papers/v1/7017147/references?page=2

API reference For AI assistants