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 *

114 related articles for article (PubMed ID: 302678)

  • 1. [Partial monosomy 11q. A new case].
    Bresson JL; Noir A
    Ann Genet; 1977 Mar; 20(1):63-6. PubMed ID: 302678
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Partial 11q monosomy and trigonocephaly. A new syndrome].
    Turleau C; Chavin-Colin F; Roubin M; Thomas D; de Grouchy TJ
    Ann Genet; 1975 Dec; 18(4):257-60. PubMed ID: 1083197
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Partial monosomy due to long-arm deletion of chromosome 11 : del (11) (q23) (author's transl)].
    Léonard C; Courpotin C; Labrune B; Lepercq G; Kachaner J; Caut P
    Ann Genet; 1979 Jun; 22(2):115-20. PubMed ID: 315201
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Monosomy 11Q: report of new phenotypic manifestations.
    Puvabanditsin S; Garrow E; Zia-Ullah MO; Supavekin S; Lianthanasarn P; Denev KI
    Genet Couns; 2001; 12(3):283-6. PubMed ID: 11693793
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Trigonocephaly and the 11q- syndrome.
    Cassidy SB; Heller RM; Kilroy AW; McKelvey W; Engel E
    Ann Genet; 1977 Mar; 20(1):67-9. PubMed ID: 302679
    [TBL] [Abstract][Full Text] [Related]  

  • 6. De novo partial 2q3 trisomy/distal 7p22 monosomy in a malformed newborn with 7p deletion phenotype and craniosynostosis.
    Fryns JP; Haspeslagh M; Agneessens A; van den Berghe H
    Ann Genet; 1985; 28(1):45-8. PubMed ID: 3874588
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial monosomy of the long arm of chromosome 11 in a severely affected child.
    Lee ML; Sciorra LJ
    Ann Genet; 1981; 24(1):51-3. PubMed ID: 6971620
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Partial monosomy 10p syndrome.
    Koenig R; Kessel E; Schoenberger W
    Ann Genet; 1985; 28(3):173-6. PubMed ID: 3879152
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Partial deletion of the short arm of the chromosome 9].
    Serville F; Allain D; Broustet A; Martin C; Gachet M; Babin JP; Cenraud J
    Ann Genet; 1976 Jun; 19(2):143. PubMed ID: 1085605
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Two new cases of partial monosomy 11q with breakpoint in 11q24 (author's transl)].
    Laurent C; Biemont MC; Veyron M; Guilhot J; Guibaud P
    Ann Genet; 1979; 22(4):239-41. PubMed ID: 317789
    [No Abstract]   [Full Text] [Related]  

  • 11. A case of partial 9p monosomy with some unusual clinical features.
    Rutten FJ; Hustinx TW; Dunk-Tillemans AA; Scheres JM; Tjon YS
    Ann Genet; 1978 Mar; 21(1):51-5. PubMed ID: 308344
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [De novo monosomy 4q32.1 leads to 4qter in a newborn with multiple malformations (author's transl)].
    Rethoré MO; Couturier J; Mselati JC; Cochois B; Lavaud J; Lejeune J
    Ann Genet; 1979; 22(4):214-6. PubMed ID: 317783
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11q.
    Cousineau AJ; Higgins JV; Scott-Emuakpor AB; Mody G
    Am J Med Genet; 1983 Jan; 14(1):29-35. PubMed ID: 6829609
    [TBL] [Abstract][Full Text] [Related]  

  • 14. De novo del(7)(pter----p21.2::p15.2----qter) and craniosynostosis. Implications for critical segment assignment in the 7p2 monosomy syndrome.
    García-Esquivel L; García-Cruz D; Rivera H; Plascencia ML; Cantú JM
    Ann Genet; 1986; 29(1):36-8. PubMed ID: 3487273
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Monosomy 7qter (author's transl)].
    Lambert JC; Mariani R; Donzeau M; Ferrari M; Boutte P; Ayraud N
    Arch Fr Pediatr; 1981 Mar; 38(3):177-80. PubMed ID: 7235841
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Monosomy 11q: report of two familial cases and review of the literature.
    Hustinx R; Verloes A; Grattagliano B; Herens C; Jamar M; Soyeur D; Schaaps JP; Koulischer L
    Am J Med Genet; 1993 Sep; 47(3):312-7. PubMed ID: 8135272
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.
    Courtens W; Wauters J; Wojciechowski M; Reyniers E; Scheers S; van Luijk R; Rooms L; Kooy F; Wuyts W
    Clin Dysmorphol; 2007 Oct; 16(4):231-9. PubMed ID: 17786114
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [9p monosomy. About a new case. Clinical and cytogenetic study (author's transl)].
    Lajarrige C; Bouquier JJ; Ronayette D; Tchertoff C; Faugeras C; Barthe D; Laleu J
    Ann Pediatr (Paris); 1979 Nov; 26(9):631-6. PubMed ID: 555637
    [No Abstract]   [Full Text] [Related]  

  • 19. Two craniosynostotic patients with 11q deletions, and review of 48 cases.
    Lewanda AF; Morsey S; Reid CS; Jabs EW
    Am J Med Genet; 1995 Nov; 59(2):193-8. PubMed ID: 8588585
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Clinical picture of partial monosomy of chromosome 11 q].
    Dörr U
    Monatsschr Kinderheilkd; 1986 Nov; 134(11):808-11. PubMed ID: 3807920
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.