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 *

120 related articles for article (PubMed ID: 2526612)

  • 1. Inherited pericentric inversion of Y-chromosome with trisomy 21. A case report.
    Krishna Murthy DS; Murthy SK; Patel JK; Banker GN; Shah VC
    Ann Genet; 1989; 32(1):47-51. PubMed ID: 2526612
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [Rare structural rearrangement of the Y chromosome (Yq-,S) in the family of a boy with a sex differentiation disorder].
    Verlinskaia DK; Kovaleva NV; Prozorova MV; Khitrikova LE
    Tsitologiia; 1983 Feb; 25(2):204-6. PubMed ID: 6134363
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
    Butomo IV; Prozorova MV; Khitrikova LE
    Tsitol Genet; 1984; 18(3):223-8. PubMed ID: 6235655
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Familial pericentric inversion of the X chromosome [inv(X)(p11q28)]].
    Baumann W; Zabel B; Holl M
    Ann Genet; 1984; 27(2):106-8. PubMed ID: 6331785
    [TBL] [Abstract][Full Text] [Related]  

  • 6. True vs. false inv(Y)(p11q11.2): a familial instance concurrent with trisomy 21.
    Rivera H; Gutiérrez-Angulo M; Gómez-Sánchez H; Macías-Gómez N; Barros-Núñez P
    Ann Genet; 2002; 45(2):63-5. PubMed ID: 12119213
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial pericentric inversion of the Y chromosome.
    Tóth A; Gaál M; László J
    Ann Genet; 1984; 27(1):60-1. PubMed ID: 6609677
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. [Description of a case of ring chromosome 21 and pericentric inversion of Y chromosome].
    Ponzio G; Carozzi F; Dragone E; Spada A; Brignone S; De Marchi M; Carbonara A
    Pathologica; 1983; 75 Suppl():276-9. PubMed ID: 6680430
    [No Abstract]   [Full Text] [Related]  

  • 10. Two unbalanced segregation products due to a maternal t(7;16)inv(16).
    Leegte B; Sikkema-Raddatz B; Hordijk R; Davelaar I; van der Veen A; Cobben JM
    Prenat Diagn; 2001 Jul; 21(7):550-2. PubMed ID: 11494289
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Pericentric inversion of the Y chromosome as an exclusion constellation].
    Bullerdiek J; Bartnitzke S; Pahlke R
    Anthropol Anz; 1984 Mar; 42(1):67-72. PubMed ID: 6586109
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Double trisomy and transmitted pericentric inversion (48,XXY, +21,inv(22)). Interchromosomal effect].
    Saura R; Longy M; Sautarael M; Renouil M; Sandler B
    Ann Genet; 1983; 26(3):180-2. PubMed ID: 6606381
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Familial pericentric inversion of y chromosome and Down's syndrome].
    García Sagredo JM; Morán Cabré A; San Román Cos-Gayón C
    An Esp Pediatr; 1975; 8(1):68-71. PubMed ID: 123717
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Two Down syndrome patients with rec(21),dupq,inv(21)(p11;q2109) from a familial pericentric inversion.
    Léonard C; Gautier M; Sinet PM; Selva J; Huret JL
    Ann Genet; 1986; 29(3):181-3. PubMed ID: 2947534
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Trisomy 20p derived from a maternal pericentric inversion and brachymesophalangy of the index finger].
    Lucas J; Le Mée F; Le Marec B; Pluquailec K; Journel H; Picard F
    Ann Genet; 1985; 28(3):167-71. PubMed ID: 3879151
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pericentric inversions of the X chromosome. A new observation and review of the published cases.
    Pfeiffer RA; Kossakiewicz M; Baisch C
    J Genet Hum; 1986 Aug; 34(3-4):331-7. PubMed ID: 3760837
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Constitutional chromosome anomalies in patients with cerebral gigantism (Sotos syndrome).
    Haeusler G; Guchev Z; Köhler I; Schober E; Haas O; Frisch H
    Klin Padiatr; 1993; 205(5):351-3. PubMed ID: 8411901
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Unusual chromosomal rearrangement. An autosomal telomeric translocation on a multicentury satellited Y (Yqs) chromosome].
    Genest P; Genest FB; Gagnon-Blais D
    Ann Genet; 1983; 26(2):86-90. PubMed ID: 6604491
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Oligohydramnios syndrome and XYY karyotype.
    Côté GB; Tsomi K; Papadakou-Lagoyanni S; Petmezaki S
    Ann Genet; 1978 Dec; 21(4):226-8. PubMed ID: 314260
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial robertsonian translocation 15;21 and rare paracentric inv(21): unexpected re-inversion in a child with translocation trisomy 21.
    Mau UA; Petruch UR; Kaiser P; Eggermann T
    Eur J Hum Genet; 2000 Nov; 8(11):815-9. PubMed ID: 11093270
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.