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 *

50 related articles for article (PubMed ID: 877898)

  • 1. [Association of congenital defects of the cardiovascular system with sex development anomalies due to monosomy of X-chromosome].
    Mirzaiants GG
    Ter Arkh; 1977; 49(5):64-8. PubMed ID: 877898
    [No Abstract]   [Full Text] [Related]  

  • 2. [XXY karyotype, cardiovascular anomalies and facial dysmorphia in a 12-year-old boy].
    Emerit I; de Grouchy J; Frezal J; Josso N; Corone P; Vernant P; Soulie P; Lamy M
    Arch Fr Pediatr; 1968 May; 25(5):531-9. PubMed ID: 5738878
    [No Abstract]   [Full Text] [Related]  

  • 3. Congenital heart disease in 49, XXXXY syndrome.
    Karsh RB
    Pediatrics; 1975 Sep; 56(3):462-4. PubMed ID: 1161403
    [No Abstract]   [Full Text] [Related]  

  • 4. Penta X (49,XXXXX) chromosome constitution: a case report.
    Yamada Y; Neriishi S
    Jinrui Idengaku Zasshi; 1971 Aug; 16(1):15-21. PubMed ID: 5166615
    [No Abstract]   [Full Text] [Related]  

  • 5. [Central thyroid insufficiency in the 47, XYY syndrome].
    Lévy JM; Stoll C; Krug JP; Kupferberg J
    Pediatrie; 1975 Mar; 30(2):137-43. PubMed ID: 1129021
    [No Abstract]   [Full Text] [Related]  

  • 6. [Familial occurrence of congenital angiocardiopathies].
    Schieche M
    Z Gesamte Inn Med; 1970 Dec; 25(24):1103-8. PubMed ID: 5520023
    [No Abstract]   [Full Text] [Related]  

  • 7. Congenital heart disease in a tetra-X woman.
    Keane JF; McLennan JE; Chi JG; Monedjikova V; Vawter GF; Gilles FH; Van Praagh R
    Chest; 1974 Dec; 66(6):726-9. PubMed ID: 4279164
    [No Abstract]   [Full Text] [Related]  

  • 8. [Studies on phenotype-genotype association and X-monosomy mosaicism in the human sex differentiation abnormality].
    Handa Y
    Hokkaido Igaku Zasshi; 2002 Sep; 77(5):477-90. PubMed ID: 12404762
    [No Abstract]   [Full Text] [Related]  

  • 9. Renal anomalies in the "XY female".
    Swanson JA; Chapler FK
    Obstet Gynecol; 1978 Feb; 51(2):237-40. PubMed ID: 564007
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hypoplastic genitalia, abnormal facies and congenital heart disease.
    Kohlinsky SM; Morris D; McCarthy GT
    Proc R Soc Med; 1971 Jan; 64(1):18-9. PubMed ID: 5551440
    [No Abstract]   [Full Text] [Related]  

  • 11. [Congenital heart diseases in chromosome abnormalities. I. In Down's syndrome (mongolism)].
    Armendares S; Pérez Treviño C
    Arch Inst Cardiol Mex; 1968; 38(6):779-91. PubMed ID: 4237287
    [No Abstract]   [Full Text] [Related]  

  • 12. [Congenital lymphedema and monosomy X (author's transl)].
    Izakovic V
    Bratisl Lek Listy; 1979 Nov; 72(5):530-4. PubMed ID: 509298
    [No Abstract]   [Full Text] [Related]  

  • 13. Letter: Cytomegalovirus and penta X syndrome.
    Genoud J; Guibaud P; Bethenod M
    J Pediatr; 1974 Dec; 85(6):869. PubMed ID: 4370946
    [No Abstract]   [Full Text] [Related]  

  • 14. Congenital heart defects and chromosomal anomalies including 22q11 microdeletion (CATCH 22).
    Soares G; Alvares S; Rocha C; Teixeira MF; Mota MC; Reis MI; Feijó MJ; Lima MR; Pinto MR
    Rev Port Cardiol; 2005 Mar; 24(3):349-71. PubMed ID: 15929620
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Noonan's syndrome associated with cardiovascular anomalies; report of three cases].
    Yamauchi T; Morishita Y; Shimokawa S; Hashiguchi M; Yuda T; Taira A; Maruko O
    Kyobu Geka; 1989 Jan; 42(1):32-4. PubMed ID: 2724730
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Cytogenetic evaluation in primary amenorrhea with a clinical presumption of sex chromosome abnormality].
    de León Esparza M; Leal Garza CH; Garza Chapa R
    Ginecol Obstet Mex; 1983 Feb; 51(310):29-31. PubMed ID: 6681368
    [No Abstract]   [Full Text] [Related]  

  • 17. Congenital heart disease and its association with other congenital malformations found at autopsy.
    Davies BR; Rizo T; Arroyo-Valerio A
    Pediatr Pathol Mol Med; 2002; 21(6):541-9. PubMed ID: 12537771
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Klinefelter's syndrome among offspring of women with triple-X anomaly.
    Zizka J; Nielsen J; Balícek P
    Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove Suppl; 1975; 19(1):177-82. PubMed ID: 1071485
    [No Abstract]   [Full Text] [Related]  

  • 19. Speech and language development in 41 children with sex chromosome anomalies.
    Bender B; Fry E; Pennington B; Puck M; Salbenblatt J; Robinson A
    Pediatrics; 1983 Feb; 71(2):262-7. PubMed ID: 6823432
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Sperm sex chromosome analysis and preimplantation genetic diagnosis of patients with sex chromosome anomalies].
    Xu YW; Ren XL; Zhou CQ; Li HP; Liu Y; Zhang MF; Zhuang GL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Aug; 23(4):431-3. PubMed ID: 16883533
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.