These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 6681937)

  • 1. Duplication (17p) in a child with an isodicentric (17p) chromosome.
    Mascarello JT; Jones MC; Hoyme HE; Freebury MM
    Am J Med Genet; 1983 Jan; 14(1):67-72. PubMed ID: 6681937
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies.
    Elejalde BR; Opitz JM; de Elejalde MM; Gilbert EF; Abellera M; Meisner L; Lebel RR; Hartigan JM
    Am J Med Genet; 1984 Apr; 17(4):723-30. PubMed ID: 6539070
    [TBL] [Abstract][Full Text] [Related]  

  • 3. De novo partial 2p duplication with postmortem description.
    Monteleone PL; Blair JD; Graviss ER; Chen SC; Salvador A; Grzegocki JA; Monteleone JA
    Am J Med Genet; 1981; 10(1):55-64. PubMed ID: 7197468
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Monosomy 21: a possible stepwise evolution of the karyotype.
    Abeliovich D; Carmi R; Karplus M; Bar-Ziv J; Cohen MM
    Am J Med Genet; 1979; 4(3):279-86. PubMed ID: 574719
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fetal manifestation of a chromosomal disorder: partial duplication of the long arm of chromosome 5 (5q33 to qter).
    Passarge E; Bartsch-Sandhoff M; Rehder H
    Teratology; 1982 Apr; 25(2):221-5. PubMed ID: 7101200
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
    Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Interstitial deletion of the long arm of one 11 chromosome].
    Taillemite JL; Morlier BG; Roux C
    Ann Genet; 1975 Mar; 18(1):61-3. PubMed ID: 1080039
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evidence for involvement of a Robertsonian translocation 13 chromosome in formation of a ring chromosome 13.
    Stetten G; Tuck-Muller CM; Blakemore KJ; Wong C; Kazazian HH; Antonarakis SE
    Mol Biol Med; 1990 Dec; 7(6):479-84. PubMed ID: 2077349
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis and characterization of an analphoid marker chromosome 16.
    Tabet AC; Gosset P; Elghezal H; Fontaine S; Martinovic J; Encha Razavi F; Romana S; Vekemans M; Morichon-Delvallez N
    Prenat Diagn; 2004 Sep; 24(9):733-6. PubMed ID: 15386469
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Isodicentric chromosome 18 in an abnormal infant using chromosome specific DNA probe.
    Meguid NA; Habibian R
    Clin Genet; 1992 May; 41(5):225-8. PubMed ID: 1606710
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interstitial dup(1p) and severe intrauterine growth retardation.
    Dhellemmes C; Choiset A; Narbouton R; Girard S; Tapia S; Thepot F; Sarrut S
    Ann Genet; 1988; 31(2):129-31. PubMed ID: 3261150
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Brief clinical report: deletion of the long arm of chromosome 11, [del(11)(q23)].
    Monteleone PL; Chen SC; Nouri-Moghaddam S; Blair JD; Tietjens M
    Am J Med Genet; 1982 Nov; 13(3):299-304. PubMed ID: 6891182
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Morphologic abnormality due to duplication of chromosome 17 (46,XY,17q+) in a newborn infant].
    Fouquette B; Rosenfeld R; Cadotte M
    Union Med Can; 1974 Aug; 103(8):1404-8. PubMed ID: 4849205
    [No Abstract]   [Full Text] [Related]  

  • 14. De novo duplication of 17p [dup(17)(p12----p11.2)]: report of an additional case with confirmation of the cytogenetic, phenotypic, and developmental aspects.
    Kozma C; Meck JM; Loomis KJ; Galindo HC
    Am J Med Genet; 1991 Dec; 41(4):446-50. PubMed ID: 1776635
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Tetrasomy of the short arm of human chromosome 18: cytogenetics and phenotypic disorders].
    Kuleshov NP; Zaletaev DV; Levina LIa; Dement'eva GM; Arbuzov SP
    Tsitol Genet; 1985; 19(6):452-6. PubMed ID: 4089954
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
    Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature.
    de Die-Smulders CE; Engelen JJ; Schrander-Stumpel CT; Govaerts LC; de Vries B; Vles JS; Wagemans A; Schijns-Fleuren S; Gillessen-Kaesbach G; Fryns JP
    Am J Med Genet; 1995 Nov; 59(3):369-74. PubMed ID: 8599364
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Duplication of 16p from insertion of 16p into 16q with subsequent duplication due to crossing over within the inserted segment.
    Cohen MM; Lerner C; Balkin NE
    Am J Med Genet; 1983 Jan; 14(1):89-96. PubMed ID: 6829613
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.
    Hsia YE; Appadorai V; Breg WR; Howard RO
    Birth Defects Orig Artic Ser; 1974; 10(8):19-25. PubMed ID: 4142400
    [No Abstract]   [Full Text] [Related]  

  • 20. The dup(3q) syndrome: report of eight cases and review of the literature.
    Steinbach P; Adkins WN; Caspar H; Dumars KW; Gebauer J; Gilbert EF; Grimm T; Habedank M; Hansmann I; Herrmann J; Kaveggia EG; Langenbeck U; Meisner LF; Najafzadeh TM; Opitz JM; Palmer CG; Peters HH; Scholz W; Tavares AS; Wiedeking C
    Am J Med Genet; 1981; 10(2):159-77. PubMed ID: 7315873
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.