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Paper640658

Partial trisomy 10p in two generations.

Lurie IW and 5 others. Hum Genet, 1978. Cited by 29 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Partial trisomy 10p in two generations. Papers, record 640658. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/640658

Paper

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

Title
Partial trisomy 10p in two generations.
PubMed
Journal
Hum Genet
PubMed
Year
1978
PubMed
Publication types
Case Reports, Journal Article
PubMed
Citations, by iCite
29
iCite
Relative citation ratio, by iCite
2.2
iCite
Revised in PubMed
2019-07-22
PubMed

Authors6

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

OrderAuthorForenameKindORCID iD
1Lurie IWI W
2Lazjuk GIG I
3Gurevich DBD B
4Kravtzoa GIG I
5Nedzved MKM K
6Shved IAI A

Source PubMed

Topics14

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

MeSH termMajor
Chromosomes, Human, 6-12 and XMajor topic
TrisomyMajor topic
Adult
Cleft Lip
Cleft Palate
Clubfoot
Female
Humans
Infant, Newborn
Karyotyping
Male
Pedigree
Polycystic Kidney Diseases
Skull

Source PubMed

References13

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

OrderPMIDTitleJournalYearIn PapersSource
11,086,628[2 cases of partial trisomy 10p due to a paternal translocation t(10p;18)(p13;q23)].Ann Genet1976https://conductscience.org/library/papers/1086628PubMed
24,270,654Precise identification of various chromosomal abnormalities.Ann Hum Genet1973https://conductscience.org/library/papers/4270654PubMed
31,080,038Trisomy iop. A report of two cases due to a familial translocation rcp (10;21) (pII;pII).Ann Genet1975https://conductscience.org/library/papers/1080038PubMed
44,434,655Trisomy for the short arm of chromosome No. 10.Clin Genet1974https://conductscience.org/library/papers/4434655PubMed
51,150,239Exclusion gene mapping utilizing patients with chromosome imbalance: the HL-A system as a prototype.Humangenetik1975https://conductscience.org/library/papers/1150239PubMed
61,176,136Partial trisomy 10p.Humangenetik1975https://conductscience.org/library/papers/1176136PubMed
75,464,693[A case of multiple congenital anomalies with familial C-G translocation].Jinrui Idengaku Zasshi1970https://conductscience.org/library/papers/5464693PubMed
8844,878Partial trisomy 10p and familial translocation t(7;10)(p22;p12).Hum Genet1977https://conductscience.org/library/papers/844878PubMed
91,219,122Trisomy of the short arm of chromosome 10.J Med Genet1975https://conductscience.org/library/papers/1219122PubMed
101,084,124Trisomy iop.Ann Genet1976https://conductscience.org/library/papers/1084124PubMed
114,844,639Brother and sister with trisomy 10p: a new syndrome.Humangenetik1974https://conductscience.org/library/papers/4844639PubMed
121,084,125[Trisomy 10 p. A previously reported case explained by binding].Ann Genet1976https://conductscience.org/library/papers/1084125PubMed
135,303,428An intersexual infant with an extra chromosome.Ann Genet1968https://conductscience.org/library/papers/5303428PubMed

Cited by11

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 29 citations.

PMIDTitleJournalYearIn PapersSource
34,513,343Goyal-Naqvi Syndrome (Concurrent Trisomy 10p and Terminal 14q Deletion): A Review of the Literature.Cureus2021https://conductscience.org/library/papers/34513343PubMed
17,436,238Genetic factors in congenital diaphragmatic hernia.Am J Hum Genet2007https://conductscience.org/library/papers/17436238PubMed
7,450,764Reciprocal translocations: a way to predict the mode of imbalanced segregation by pachytene-diagram drawing.Hum Genet1980https://conductscience.org/library/papers/7450764PubMed
7,262,871Duplication deficiency as the result of meiotic segregation of a maternal InV (10).Hum Genet1981https://conductscience.org/library/papers/7262871PubMed
7,151,837Two chromosomal syndromes in the same family: monosomy and trisomy for part of the short arm of chromosome 10.Eur J Pediatr1982https://conductscience.org/library/papers/7151837PubMed
6,842,544Partial monosomy of chromosome 10 short arms.J Med Genet1983https://conductscience.org/library/papers/6842544PubMed
2,746,620A case of two inversion (10) recombinants in a family.J Med Genet1989https://conductscience.org/library/papers/2746620PubMed
468,260Increased HK1 activity levels in the red cells of a patient with a de novo trisomy 10p: t(Y;10)(p11;p12).Hum Genet1979https://conductscience.org/library/papers/468260PubMed
437,788Partial duplication of the short arm of chromosome 10. Karyotype: 46,XX,dup(10p)(pter to p12::p12::p12 to qter).Hum Genet1979https://conductscience.org/library/papers/437788PubMed
422,195Trisomy 10p due to a de novo t(10p;13p).Hum Genet1979https://conductscience.org/library/papers/422195PubMed
395,305Factors predisposing to adjacent 2 and 3:1 disjunctions: study of 161 human reciprocal translocations.J Med Genet1979https://conductscience.org/library/papers/395305PubMed

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

None in this release

  • Grants
  • Trials
  • Comments and corrections
  • Genes
  • Drugs
  • Data

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.

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