Home LiteratureArticle Details
PMID: 2187342 Published · ppublish English Comment Journal Article Research Support, U.S. Gov't, P.H.S. Review

Mapping dysmorphic syndromes with the aid of the human/mouse homology map.

American journal of human genetics ·Vol. 46 ·No. 6 ·1990-06-00 ·Pages 1013-6

Erickson RP

Abstract

暂无摘要

MeSH Terms
Abnormalities, Multiple/genetics Animals Chromosome Mapping DNA/genetics Humans Mice Sequence Homology, Nucleic Acid Syndrome Waardenburg Syndrome/genetics
Chemicals
DNA
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Erickson R P
Department of Human Genetics, University of Michigan Medical School, Ann Arbor 48109-0718.
References (25)
25 references, click to expand
  1. X-linked genetic homologies between mouse and man.
    Genomics. 1987 Nov;1(3):213-27 PMID: 3328737
  2. Two cases of X/autosome translocation in females with incontinentia pigmenti.
    Hum Genet. 1985;71(3):231-4 PMID: 4065895
  3. Altered copper metabolism in cultured cells from human Menkes' syndrome and mottled mouse mutants.
    Biochem Genet. 1980 Feb;18(1-2):117-31 PMID: 7387619
  4. Abnormal ornithine carbamoyltransferase in mice having the sparse-fur mutation.
    Proc Natl Acad Sci U S A. 1976 May;73(5):1693-7 PMID: 5727
  5. Gene for incontinentia pigmenti maps to band Xp11 with an (X;10) (p11;q22) translocation.
    Clin Genet. 1987 Jul;32(1):66-9 PMID: 3621656
  6. Anhidrosis and absence of sweat glands in mice hemizygous for the Tabby gene: supportive evidence for the hypothesis of homology between Tabby and human anhidrotic (hypohidrotic) ectodermal dysplasia (Christ-Siemens-Touraine syndrome).
    J Invest Dermatol. 1986 Dec;87(6):720-2 PMID: 3782855
  7. Chromosome maps of man and mouse. IV.
    Ann Hum Genet. 1989 May;53(Pt 2):89-140 PMID: 2688541
  8. The Controlling Element in Sex Chromosome Behavior in Sciara.
    Genetics. 1960 Oct;45(10):1429-43 PMID: 17248010
  9. Greig cephalopolysyndactyly syndrome: a possible mouse homologue (Xt-extra toes).
    Am J Med Genet. 1988 Dec;31(4):793-8 PMID: 3239570
  10. The molars of the tabby mouse, and a test of the 'single-active X-chromosome' hypothesis.
    J Embryol Exp Morphol. 1966 Apr;15(2):223-44 PMID: 5959976
  11. Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X chromosome.
    N Engl J Med. 1984 Oct 18;311(16):1010-5 PMID: 6482910
  12. A mouse malformation mutant supplement to the London Dysmorphology Database.
    Am J Med Genet. 1988 Jul;30(3):819-20 PMID: 3189401
  13. Waardenburg syndrome type I in a child with de novo inversion (2)(q35q37.3).
    Am J Med Genet. 1989 Aug;33(4):505-7 PMID: 2596512
  14. Familial aniridia and translocation t(4;11)(q22;p13) without Wilms' tumor.
    Hum Genet. 1983;63(2):158-61 PMID: 6301974
  15. Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouse.
    Am J Hum Genet. 1990 Jun;46(6):1017-23 PMID: 2339698
  16. A compendium of the genetically induced congenital malformations of the house mouse.
    Teratology. 1980 Jun;21(3):397-429 PMID: 7455930
  17. Homologous genes for X-linked chondrodysplasia punctata in man and mouse.
    Hum Genet. 1983;63(1):24-7 PMID: 6682087
  18. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion.
    Am J Med Genet. 1989 Feb;32(2):285-90 PMID: 2564739
  19. Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11.
    Hum Genet. 1988 Nov;80(3):282-6 PMID: 3192215
  20. Chromosomal imprinting and the parent transmission specific variation in expressivity of Huntington disease.
    Am J Hum Genet. 1985 Jul;37(4):827-9 PMID: 9556671
  21. Directed genetic change model for X chromosome inactivation in eutherian mammals.
    Nature. 1971 Apr 2;230(5292):292-4 PMID: 5549404
  22. Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.
    Nature. 1989 Nov 16;342(6247):281-5 PMID: 2812027
  23. Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse.
    Nature. 1975 Aug 21;256(5519):640-2 PMID: 1152998
  24. Pleiotropic effect of Tabby gene on epidermal growth factor-containing cells of mouse submandibular gland.
    Anat Rec. 1983 Sep;207(1):25-9 PMID: 6605698
  25. The neural crest and the acoustic ganglion.
    J Embryol Exp Morphol. 1967 Jun;17(3):533-41 PMID: 6049665
Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
1990-06-00
Pages
1013-6
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC1683848
Subset
IM
Grants
NICHD NIH HHS · HD26454 · United States
Corrections
CommentOn
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]