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 *

174 related articles for article (PubMed ID: 314260)

  • 21. A 7q- son of an XYY father.
    Kajii T; Murano I
    Jinrui Idengaku Zasshi; 1984 Sep; 29(3):387-9. PubMed ID: 6533358
    [No Abstract]   [Full Text] [Related]  

  • 22. 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]  

  • 23. Unusual chromosome aberrations in 3 children with Down syndrome.
    Osztovics M; Tóth S; Wilhelm O
    Acta Paediatr Acad Sci Hung; 1982; 23(3):283-9. PubMed ID: 6217717
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [XYY syndrome in a 15-year-old boy].
    Vuković D; Gubas-Turcan L; Krstić A
    Med Pregl; 1978; 31(5-6):215-9. PubMed ID: 672802
    [No Abstract]   [Full Text] [Related]  

  • 25. [XYY syndrome: report of three cases].
    Okamoto E; Yabumoto H; Terakawa T; Shima H; Ikoma F; Sakamoto H; Furuyama J
    Hinyokika Kiyo; 1988 Jan; 34(1):191-5. PubMed ID: 3287855
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Effects of the Y chromosome on quantitative growth: an anthropometric study of 47,XYY males.
    Varrela J; Alvesalo L
    Am J Phys Anthropol; 1985 Oct; 68(2):239-45. PubMed ID: 4061613
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Incidence of 47,XYY karyotype in a consecutive series of newborn males in Tokyo.
    Iijima K; Higurashi M; Hirayama M
    Hum Genet; 1978 Aug; 43(2):211-4. PubMed ID: 689687
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The XYY genotype.
    Walzer S; Gerald PS; Shah SA
    Annu Rev Med; 1978; 29():568-70. PubMed ID: 348046
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Chromosomes and violence.
    Pitcher DR
    Practitioner; 1982 Mar; 226(1365):497-501. PubMed ID: 7088840
    [No Abstract]   [Full Text] [Related]  

  • 30. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
    Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I
    Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Acute myelomonocytic leukemia with inv(16) (p13q22) developed in an XY/XYY male].
    Iwabuchi H; Lin KY; Ohyashiki JH; Ohyashiki K; Toyama K
    Rinsho Ketsueki; 1987 Dec; 28(12):2204-8. PubMed ID: 3483028
    [No Abstract]   [Full Text] [Related]  

  • 32. [XYY syndrome (diplo-Y syndrome)].
    Braun-Scharm H; Schroeder-Kurth TM
    Z Kinder Jugendpsychiatr; 1986; 14(2):175-83. PubMed ID: 3799086
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Summary of clinical findings: profiles of children with 47,XXY, 47,XXX and 47,XYY karyotypes.
    Robinson A; Lubs HA; Nielsen J; Sørensen K
    Birth Defects Orig Artic Ser; 1979; 15(1):261-6. PubMed ID: 444644
    [No Abstract]   [Full Text] [Related]  

  • 34. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY
    Am J Med Genet; 1994 Nov; 53(2):108-40. PubMed ID: 7856637
    [TBL] [Abstract][Full Text] [Related]  

  • 35. What is to be done with the XYY fetus.
    Wilkinson S
    Br Med J; 1979 Jul; 2(6182):131. PubMed ID: 466308
    [No Abstract]   [Full Text] [Related]  

  • 36. Prenatal detection of the 47, XYY karyotype.
    Goldenberg RL; Finley SC
    Lancet; 1978 Aug; 2(8087):465-6. PubMed ID: 79819
    [TBL] [Abstract][Full Text] [Related]  

  • 37. An adult with 49,XYYYY karyotype: case report and endocrine studies.
    Shanske A; Sachmechi I; Patel DK; Bishnoi A; Rosner F
    Am J Med Genet; 1998 Nov; 80(2):103-6. PubMed ID: 9805123
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Indications for chromosome analysis].
    Pfeiffer RA
    Fortschr Med; 1985 Jan; 103(3):33-6. PubMed ID: 3156080
    [No Abstract]   [Full Text] [Related]  

  • 39. The 47,xyy karyotype in a 14-year-old boy with normal stature coming from a maladjusted family with history of schizophrenia.
    Zizka J; Balícek P; Krenová I; Hametová M
    Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove Suppl; 1977; 20(4):495-9. PubMed ID: 306679
    [No Abstract]   [Full Text] [Related]  

  • 40. [C-G translocation: karyotype 46, XY,t(Cq-; Gq+): parents 46, XX and 46, XY].
    Lambotte C; Carlier G; Frederic J; Keutgen J
    Acta Paediatr Belg; 1971; 25(2):119-26. PubMed ID: 5565831
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.