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 *

132 related articles for article (PubMed ID: 4035270)

  • 1. 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]  

  • 2. An infant with double trisomy (48,XXX, + 18).
    Jaruratanasirikul S; Jinorose U
    Am J Med Genet; 1994 Jan; 49(2):207-10. PubMed ID: 8116670
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Penta-X syndrome. Report of a case with 47,XXX/48,XXXX/49,XXXXX mosaicism].
    Gómez-Valencia L; Nájera-Martínez P; Morales-Hernández A; Martínez-Díaz De León A
    Bol Med Hosp Infant Mex; 1989 Jun; 46(6):417-21. PubMed ID: 2665783
    [TBL] [Abstract][Full Text] [Related]  

  • 4. ["Superfemale syndrome" in a 12-year-old girl (XXXX sex chromosome arrangement) associated with a combination of congenital abnormalities].
    Halikowski B; Kleczkowska A; Gościńska Z; Knaus A
    Pediatr Pol; 1969 Sep; 44(9):1147-54. PubMed ID: 5364501
    [No Abstract]   [Full Text] [Related]  

  • 5. [Tetra-X syndrome with epilepsy, mental retardation and multiple dysmorphias].
    Fehlow P; Miosge W; Walther F
    Klin Padiatr; 1993; 205(2):127-9. PubMed ID: 8487481
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [48, XXXX syndrome in a fourteen year old girl].
    Lejeune J; Abonyi D
    Ann Genet; 1968 Jun; 11(2):117-9. PubMed ID: 5303423
    [No Abstract]   [Full Text] [Related]  

  • 7. Pentasomy X: report of patient and studies of X-inactivation.
    Funderburk SJ; Valente M; Klisak I
    Am J Med Genet; 1981; 8(1):27-33. PubMed ID: 7246603
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Pentasomy X: a clinical case report].
    Favetta S; Artino R; Ponzio G; Restagno G
    Pediatr Med Chir; 1992; 14(5):551-4. PubMed ID: 1362611
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A 48,XXXX female with absence of ovaries.
    Collen RJ; Falk RE; Lippe BM; Kaplan SA
    Am J Med Genet; 1980; 6(4):275-8. PubMed ID: 7211945
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [48,XXXX syndrome in a 1-year-old girl].
    Borzani M; Adamoli L; Longhi R; Nocera G; Tibiletti MG
    Minerva Pediatr; 1982 Jul 15-31; 34(13-14):621-6. PubMed ID: 6811843
    [No Abstract]   [Full Text] [Related]  

  • 11. Multiple congenital anomalies associated with a 47,XXX chromosome constitution.
    Hood OJ; Hartwell EA; Shattuck KE; Rosenberg HS
    Am J Med Genet; 1990 May; 36(1):73-5. PubMed ID: 2333909
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. [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]  

  • 14. Double trisomy 48,XXX,+ 18 in a newborn.
    Rosenfeld W; Verma RS; Jhaveri RC; Salazar D; Dosik H
    Am J Med Genet; 1981; 8(1):67-71. PubMed ID: 7246607
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 49, XXXXY syndrome in a 1 year-old infant.
    Molska I; Lech H; Wiśniewski L
    Klin Padiatr; 1977 Nov; 189(6):477-81. PubMed ID: 563945
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [48, XXXX syndrome in a 5-year-old child].
    Larget-Piet L; Pignier J; Berthelot J; Ayache P; Bourdon P; Larget-Piet A
    Pediatrie; 1972 Jun; 27(4):433-43. PubMed ID: 5071496
    [No Abstract]   [Full Text] [Related]  

  • 17. De novo direct duplication 7p (p11.2-->pter) in an Arab child with MCA/MR syndrome: trisomy 7p a delineated syndrome?
    Redha MA; Krishna Murthy DS; al-Awadi SA; al-Sulaiman IS; Sabry MA; el-Bahey SA; Farag TI
    Ann Genet; 1996; 39(1):5-9. PubMed ID: 9297445
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pigtailed macaques (Macaca nemestrina) with trisomy X manifest physical and mental retardation.
    Ruppenthal GC; Caffery SA; Goodlin BL; Sackett GP; Vigfusson NV; Peterson VG
    Am J Ment Defic; 1983 Mar; 87(5):471-6. PubMed ID: 6682289
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Distinct phenotype in maternal uniparental disomy of chromosome 14.
    Healey S; Powell F; Battersby M; Chenevix-Trench G; McGill J
    Am J Med Genet; 1994 Jun; 51(2):147-9. PubMed ID: 8092191
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Penta X syndrome: a case report with review of the literature.
    Kassai R; Hamada I; Furuta H; Cho K; Abe K; Deng HX; Niikawa N
    Am J Med Genet; 1991 Jul; 40(1):51-6. PubMed ID: 1887850
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.