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 *

274 related articles for article (PubMed ID: 7367071)

  • 1. [Case of chromosome X pentasomy].
    Sito A; Krzyzanowska J; Hofman H; Witkowska J; Sioch R; Mroczek-Orłow T
    Pediatr Pol; 1980 Jan; 55(1):77-80. PubMed ID: 7367071
    [No Abstract]   [Full Text] [Related]  

  • 2. De novo deletion of chromosome 9 (9p-) in a child with multiple congenital anomalies and psychomotor retardation.
    Murthy DS; Murthy SK; Banker GJ; Patel AJ
    Indian Pediatr; 1991 May; 28(5):546-9. PubMed ID: 1684352
    [No Abstract]   [Full Text] [Related]  

  • 3. [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]  

  • 4. [49,XXXXY syndrome in a 5-year-old boy].
    Wiśniewski L; Krajewska-Walasek M; Lech H; Mospinek M
    Pediatr Pol; 1980 Jan; 55(1):81-6. PubMed ID: 7189276
    [No Abstract]   [Full Text] [Related]  

  • 5. [Interstitial deletion of the long arm of one 11 chromosome].
    Taillemite JL; Morlier BG; Roux C
    Ann Genet; 1975 Mar; 18(1):61-3. PubMed ID: 1080039
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ring chromosome 15 syndrome.
    Fryns JP; Jaeken J; Devlieger H; Debucquoy P; Eggermont E; Van den Berghe H
    Acta Paediatr Belg; 1981; 34(1):47-9. PubMed ID: 7270144
    [No Abstract]   [Full Text] [Related]  

  • 7. [Chromosome 8 trisomy in an infant].
    Rogóyski A; Babel M; Tronowska TD
    Pediatr Pol; 1982; 57(5-6):425-7. PubMed ID: 7155694
    [No Abstract]   [Full Text] [Related]  

  • 8. [Bone malformations associated with deletion of the long arm of chromosome X].
    Hurgoiu V; Suciu S; Nicoară Z; Florescu P; David-Mark S
    Rev Pediatr Obstet Ginecol Pediatr; 1988; 37(4):373-6. PubMed ID: 3150606
    [No Abstract]   [Full Text] [Related]  

  • 9. [Morphologic abnormality due to duplication of chromosome 17 (46,XY,17q+) in a newborn infant].
    Fouquette B; Rosenfeld R; Cadotte M
    Union Med Can; 1974 Aug; 103(8):1404-8. PubMed ID: 4849205
    [No Abstract]   [Full Text] [Related]  

  • 10. Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.
    Hsia YE; Appadorai V; Breg WR; Howard RO
    Birth Defects Orig Artic Ser; 1974; 10(8):19-25. PubMed ID: 4142400
    [No Abstract]   [Full Text] [Related]  

  • 11. [48,XXYY syndrome in a boy with essential tremor. Comparison with 120 cases from the literature].
    Donati F; Gasser S; Mullis P; Braga S; Vassella F
    Monatsschr Kinderheilkd; 1992 Apr; 140(4):216-9. PubMed ID: 1614446
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Fetal triploidy--diagnosis and sequelae].
    Hauschild R; Beensen V; Eichhorn KH; Schulze E
    Zentralbl Gynakol; 1991; 113(2):111-3. PubMed ID: 2042423
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Importance of chromosomal satellites].
    Rosenkranz W; Glatzl J; Holzer S
    Wien Klin Wochenschr; 1972 Nov; 84(45):725-7. PubMed ID: 4404500
    [No Abstract]   [Full Text] [Related]  

  • 14. [A new case of pentasomy X].
    Schroeter C; Jährig K; Weinke I
    Helv Paediatr Acta; 1980 Jul; 35(3):233-41. PubMed ID: 6773908
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. [Complete triploidy in a liveborn premature (author's transl)].
    Rico S; Skinner C; Lechuga JL; Fernández E; Serrano J; Casanova M; Argemí J; López A; Castro JM
    An Esp Pediatr; 1980 Jan; 13(1):71-80. PubMed ID: 7189392
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Familial Russell-syndrome (author's transl)].
    Schwingshackl A; Ganner E; Hammerer I
    Padiatr Padol; 1974; 9(2):130-7. PubMed ID: 4823694
    [No Abstract]   [Full Text] [Related]  

  • 18. Freeman Sheldon syndrome in a newborn (whistling face)--a case report.
    Rao SS; Chary R; Karan S
    Indian Pediatr; 1979 Mar; 16(3):291-2. PubMed ID: 110675
    [No Abstract]   [Full Text] [Related]  

  • 19. Preaxial acrofacial dysostosis (Nager syndrome) associated with an inherited and apparently balanced X;9 translocation: prenatal and postnatal late replication studies.
    Zori RT; Gray BA; Bent-Williams A; Driscoll DJ; Williams CA; Zackowski JL
    Am J Med Genet; 1993 Jun; 46(4):379-83. PubMed ID: 8357008
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Ring chromosome 18. 18p-/18q- -deletion-syndrome].
    Kunze J; Stephan E; Tolksdorf M
    Humangenetik; 1972; 15(4):289-318. PubMed ID: 4565746
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 14.