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 *

82 related articles for article (PubMed ID: 1251485)

  • 1. [13q syndrome. Deletion of the long arm of chromosome No. 13].
    Andersen EA; Mikkelsen M
    Ugeskr Laeger; 1976 Jan; 138(4):227. PubMed ID: 1251485
    [No Abstract]   [Full Text] [Related]  

  • 2. [13q syndrome--partial monosomy of the long arm of chromosome 13].
    Mücke J; Sandig KR; Trautmann U
    Klin Padiatr; 1983; 195(5):361-4. PubMed ID: 6685211
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J; Plaza J; Geán E
    An Esp Pediatr; 1981 Nov; 15(5):469-73. PubMed ID: 7332149
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Interstitial deletion of long arm of chromosome 13.
    Carnevale A; Frias S; Alcantar R
    Ann Genet; 1984; 27(1):49-52. PubMed ID: 6609673
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Deletion of the short arm of chromosome 18, holoprosencephaly and pitressin-sensitive diabetes insipidus].
    Noseda J; Valdes L; Caille B; Roy C; Harpey JP
    Ann Pediatr (Paris); 1985 May; 32(5):447-50. PubMed ID: 4026140
    [No Abstract]   [Full Text] [Related]  

  • 6. [Wolf syndrome. Apropos of 2 cases].
    García González P; Pedraz García C; Merino Marcos L; Salazar Veloz J; Escudero Bueno G; Salazar Villalobos V
    An Esp Pediatr; 1983 Feb; 18(2):113-7. PubMed ID: 6881733
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [13q+ chromosome due to a probable translocation of a supernumerary Y].
    Gilgenkrantz S; Pierson M; Mauuary G
    Ann Genet; 1973 Sep; 16(3):167-72. PubMed ID: 4543205
    [No Abstract]   [Full Text] [Related]  

  • 8. Genetic haploinsufficiency as a phenotypic determinant of a deletion 13q syndrome.
    Kasyan AG; Benirschke K
    Pediatr Dev Pathol; 2005; 8(6):658-65. PubMed ID: 16328665
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases].
    Destiné ML; Punnett HH; Thovichit S; DiGeorge AM; Weiss L
    Ann Genet; 1967 Jun; 10(2):65-9. PubMed ID: 5298975
    [No Abstract]   [Full Text] [Related]  

  • 10. [A short arm deletion of chromosome 13].
    Emerit I; de Grouchy J; German J
    Ann Genet; 1968 Sep; 11(3):184-6. PubMed ID: 5304619
    [No Abstract]   [Full Text] [Related]  

  • 11. Interstitial del(13q) associated with blindness and mental retardation.
    Juberg RC; Mowrey PN
    Am J Med Genet; 1984 Mar; 17(3):609-13. PubMed ID: 6711612
    [TBL] [Abstract][Full Text] [Related]  

  • 12. New chromosomal syndromes. III. The 13q deletion syndrome.
    Fryns JP; Peeters R; Petit P; Van den Berghe H
    Acta Paediatr Belg; 1980; 33(4):261-4. PubMed ID: 7282358
    [No Abstract]   [Full Text] [Related]  

  • 13. [Partial deletion of the short arm of chromosome 4 (the Wolf-Hirschhorn syndrome) with reference to the neurological and electroencephalographic aspects].
    Bonaventura F; Adamoli P; Bernardini E; Branchi M; Siani A; Bonora G
    Pediatr Med Chir; 1994; 16(4):393-8. PubMed ID: 7816704
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. A specific syndrome due to deletion of the distal long arm of chromosome 1.
    Meinecke P; Vögtel D
    Am J Med Genet; 1987 Oct; 28(2):371-6. PubMed ID: 3322005
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [The 18q-syndrome. Deletion of the long arm of chromosome nr. 18].
    Kroyer S; Niebuhr E; Vestermark S
    Ugeskr Laeger; 1974 Apr; 136(15):827. PubMed ID: 4828093
    [No Abstract]   [Full Text] [Related]  

  • 17. Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37).
    Gorski JL; Cox BA; Kyine M; Uhlmann W; Glover TW
    Am J Med Genet; 1989 Mar; 32(3):350-2. PubMed ID: 2729355
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Preliminary definition of a "critical region" of chromosome 13 in q32: report of 14 cases with 13q deletions and review of the literature.
    Brown S; Gersen S; Anyane-Yeboa K; Warburton D
    Am J Med Genet; 1993 Jan; 45(1):52-9. PubMed ID: 8418661
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cytogenetic findings in 200 children with mental retardation and multiple congenital anomalies of unknown cause.
    Coco R; Penchaszadeh VB
    Am J Med Genet; 1982 Jun; 12(2):155-73. PubMed ID: 7102722
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Interstitial deletion of the long arms of chromosome 13].
    Molina M; Santolaya JM; Onaindía ML; Sánchez E; De Gárate J
    An Esp Pediatr; 1982 Apr; 16(4):346-51. PubMed ID: 7125394
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.