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 *

117 related articles for article (PubMed ID: 7268086)

  • 1. [XXXXY syndrome: clinical-radiological findings in one patient (author's transl)].
    Ventruto V; Pisciotta R; Celona A; Cavaliere ML; Pagano L; Stabile M; Fioretti G; Togo F
    Radiol Med; 1981 Mar; 67(3):147-51. PubMed ID: 7268086
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [A newborn infant with the xxxxy-syndrome].
    Muis N; Cats BP; Ippel PF; Beemer FA
    Tijdschr Kindergeneeskd; 1982 Aug; 50(4):112-6. PubMed ID: 7135379
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 49,XXXXY: a distinct phenotype. Three new cases and review.
    Peet J; Weaver DD; Vance GH
    J Med Genet; 1998 May; 35(5):420-4. PubMed ID: 9610808
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 49,XXXXY syndrome with diabetes mellitus.
    Kim HJ; Kim D; Shin JM; Chung HK; Lee G
    Horm Res; 2006; 65(1):14-7. PubMed ID: 16357485
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Cri-du-chat syndrome and two other deformed children in a family carrying a pericentric inversion or insertion of chromosome 5].
    Delozier-Blanchet CD; Pitmon D; Schorderet D; Engel E
    J Genet Hum; 1985 Dec; 33(5):371-80. PubMed ID: 4093767
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chromosome banding studies in two patients with XXXXY syndrome.
    Levy CL; Sparkes RS; Carlson HE
    J Med Genet; 1978 Aug; 15(4):301-5. PubMed ID: 568665
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 49, XXXXY syndrome with severe vesico-ureteral reflux and hydronephrosis: report of one case.
    Chang JT; Chiu PC; Chen YY; Chao MC; Hsieh KS
    Acta Paediatr Taiwan; 2005; 46(1):35-8. PubMed ID: 16302576
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [The XXXXY syndrome. Report of 7 new cases and review of the literature (author's transl)].
    Terheggen HG; Pfeiffer RA; Haug H; Schünke W
    Z Kinderheilkd; 1973 Oct; 115(3):209-33. PubMed ID: 4203681
    [No Abstract]   [Full Text] [Related]  

  • 10. Mild intellectual deficits in a child with 49,XXXXY.
    Hersh JH; Bloom AS; Yen F; Topinka C; Weisskopf B
    Res Dev Disabil; 1988; 9(2):171-6. PubMed ID: 3406471
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Skeletal malformations caused by chromosome aberrations. Clinical and radiological study].
    Dallapiccola B; Pistocchi GF
    Minerva Med; 1972 Dec; 63(92):5049-208. PubMed ID: 4264793
    [No Abstract]   [Full Text] [Related]  

  • 12. Prepubertal XX male with profound physical and mental deficiency, retinitis pigmentosa and multiple congenital anomalies.
    Pescia G; Spahr A; Genton N; Juillard E
    Helv Paediatr Acta; 1978 Apr; 33(1):63-72. PubMed ID: 566736
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 49,XXXXX syndrome.
    Fragoso R; Hernandez A; Plascencia ML; Nazara Z; Martinez y Martinez R; Cantu JM
    Ann Genet; 1982; 25(3):145-8. PubMed ID: 6982661
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Skeletal changes in Wolf's syndrome (4p--) and in Klinefelter quadrisomy (author's transl)].
    Montanelli C; Lucchi A; Canini R; Boriani F; Pangia G; De Florio L
    Radiol Med; 1979 Nov; 65(11):807-12. PubMed ID: 554201
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. The 48, XXXX/49,XXXXY/49,XXXX,i(Yq) mosaicism in a 3-year-old boy from a twin pregnancy.
    Kaluzewski B; Podkul D; Zaborowska I; Moruzgala T; Jakubowski L
    Hum Genet; 1977 Jul; 37(3):355-9. PubMed ID: 560352
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cri du chat-syndrome in combination with partial trisomy 9 p.
    Sigmund J; Frisch H; Heinz-Erian P; Rhomberg K; Wegner RD
    Padiatr Padol; 1986; 21(1):61-7. PubMed ID: 3960564
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [XXXXY syndrome-- a clinical case].
    Youlton R; Fajnsztejn M; Cecilia Be TM
    Rev Chil Pediatr; 1981; 52(3):244-7. PubMed ID: 7198280
    [No Abstract]   [Full Text] [Related]  

  • 19. [XXXXY syndrome].
    Toudic L; L'Henoret G; Rivière D; L'Hour M; Castel Y
    Arch Fr Pediatr; 1982 Apr; 39(4):247-9. PubMed ID: 7125819
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Further magnetic resonance imaging (MRI) brain delineation of 49,XXXXY syndrome.
    Tabarki B; Shafi SA; Adwani NA; Shahwan SA
    J Child Neurol; 2012 May; 27(5):650-3. PubMed ID: 22156792
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.