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 *

101 related articles for article (PubMed ID: 1188487)

  • 1. [Presence of 2-arm Barr's body and karyotype 47 XXX in a normally intelligent 11-year-old girl with changed phenotype].
    Stojimirović E; Ajdarić B
    Srp Arh Celok Lek; 1975 May; 103(5):455-7. PubMed ID: 1188487
    [No Abstract]   [Full Text] [Related]  

  • 2. [Tetrasomy X (karyotype 48, XXXX) in a 2 and one-half year old girl].
    Izakovic V; Lukác J
    Cesk Pediatr; 1973 Feb; 28(2):77-9. PubMed ID: 4686582
    [No Abstract]   [Full Text] [Related]  

  • 3. Homicidality in a woman with a 47,XXX karyotype.
    Kazamatsuri H; Nanko S; Mato Y
    J Clin Psychiatry; 1985 Aug; 46(8):346-7. PubMed ID: 4019424
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Primary amenorrhea - relation between karyotype and phenotype].
    Diklić V; Mijin K; Tesić P; Dukić S; Devecerski M
    Srp Arh Celok Lek; 1975 Jan; 103(1):25-32. PubMed ID: 1145316
    [No Abstract]   [Full Text] [Related]  

  • 5. Feeblemindedness and XXXX karyotype.
    Di Cagno L; Franceschini P
    J Ment Defic Res; 1968 Sep; 12(3):226-36. PubMed ID: 5722467
    [No Abstract]   [Full Text] [Related]  

  • 6. [Syndrome of congenital anomalies in a girl with karyotype 47,XXX].
    Kańska B; Kleczkowska A; Knaus A; Sokolowski J; Stapińska J
    Pediatr Pol; 1971 Jan; 46(1):81-5. PubMed ID: 5545829
    [No Abstract]   [Full Text] [Related]  

  • 7. [Sex chromosome aberration with the 48 XYYY karyotype. A case report of the phenotype of a rare sex chromosome aneuploidy].
    Stein A; Heilbronner H; Jungmann J
    Z Kinder Jugendpsychiatr; 1994 Jun; 22(2):130-4. PubMed ID: 8053267
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 47,XXX/48,XXXX in a retarded three year old girl with multiple somatic anomalies.
    Ioan D; Hîrşovescu N; Dumitriu L; Belengeanu V; Muşeţeanu P; Maximilian C
    Endocrinologie; 1985; 23(2):121-4. PubMed ID: 4035270
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The fallability of X-chromatin as a screening test for anomalies of the X chromosome.
    Rary JM; Cummings D; Jones HW
    Obstet Gynecol; 1978 Jan; 51(1):107-8. PubMed ID: 619326
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. [Sex differentiation. II. Abnormalities of the sex chromosomes and changes in gonadal differentiation].
    Kofman-Alfaro S; Mutchinick O; Valdés E; Pérez-Palacios G
    Rev Invest Clin; 1984; 36(1):53-70. PubMed ID: 6371965
    [No Abstract]   [Full Text] [Related]  

  • 12. [Karyotype-phenotype correlation in a child with an idic (Yp)].
    Alvarez-Moya C; González RM; Martínez y Martínez R; Rivera H
    Bol Med Hosp Infant Mex; 1989 Jun; 46(6):414-6. PubMed ID: 2751844
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Chromosome examinations in primary amenorrhea].
    László J; Györy G
    Zentralbl Gynakol; 1969 Aug; 91(31):1001-12. PubMed ID: 5368196
    [No Abstract]   [Full Text] [Related]  

  • 14. [Sex chromosome aberrations: effect on intelligence, social adjustment and mental health].
    Forssman H
    Lakartidningen; 1970 Sep; 67(38):4293-304. PubMed ID: 4920910
    [No Abstract]   [Full Text] [Related]  

  • 15. [A 7-year-old boy with 49,XYYYY syndrome].
    Noël B; Bénézech M; Bouzon MT; Coudrot D
    Ann Genet; 1988; 31(2):111-6. PubMed ID: 3261145
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 3. Selected syndromes associated with abnormalities of the sex chromosomes.
    Wilroy RS; Summitt RL
    J Tenn Med Assoc; 1971 Apr; 64(4):318-22. PubMed ID: 5575760
    [No Abstract]   [Full Text] [Related]  

  • 17. [Studies of the chromosome pattern in Stein-Leventhal syndrome].
    Lezhava TA
    Tsitologiia; 1966; 8(2):221-9. PubMed ID: 5984071
    [No Abstract]   [Full Text] [Related]  

  • 18. Cytogenetics of müllerian agenesis. A case report.
    Jaffe SB; Loucopoulos A; Jewelewicz R
    J Reprod Med; 1992 Mar; 37(3):242-6. PubMed ID: 1564711
    [TBL] [Abstract][Full Text] [Related]  

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

  • 20. [47 XXX karyotype in a phenotypically normal 22-year-old girl].
    Malvaux P; van den Berghe H; de Visscher M
    Ann Endocrinol (Paris); 1967; 28(1):146-7. PubMed ID: 6060421
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.