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 *

74 related articles for article (PubMed ID: 3221206)

  • 1. [De novo del (13) (q31.1----qter) in a girl. Effect of gene dosage on blood coagulation factors VII and X].
    Battin J; Serville F; Mullon MH; Mateille N
    J Genet Hum; 1988 Aug; 36(4):307-14. PubMed ID: 3221206
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Structural genes of coagulation factors VII and X located on 13q34.
    Gilgenkrantz S; Briquel ME; André E; Alexandre P; Jalbert P; Le Marec B; Pouzol P; Pommereuil M
    Ann Genet; 1986; 29(1):32-5. PubMed ID: 3487272
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Linkage analysis for three coagulation factors clustering on chromosome 13q34: factor VII, factor X and protein Z.
    Vossen CY; Hasstedt SJ; Demers C; Rosendaal FR; Bovill EG
    J Thromb Haemost; 2007 Jun; 5(6):1325-7. PubMed ID: 17403098
    [No Abstract]   [Full Text] [Related]  

  • 4. Activity and antigen of coagulation factors VII and X in five patients with abnormal chromosome 13.
    Fukushima Y; Kuroki Y; Iizuka A
    Jinrui Idengaku Zasshi; 1987 Jun; 32(2):91-6. PubMed ID: 3437574
    [No Abstract]   [Full Text] [Related]  

  • 5. Interstitial deletion 8p21.3----p23.1 in a 6-year-old girl.
    Morrison PJ; Jones J; Nevin NC
    Am J Med Genet; 1992 Mar; 42(5):678-80. PubMed ID: 1632437
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
    Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
    [TBL] [Abstract][Full Text] [Related]  

  • 7. De novo del(6)(q25) associated with macular degeneration.
    Rivas F; Ruiz C; Rivera H; Möller M; Serrano-Lucas JI; Cantú JM
    Ann Genet; 1986; 29(1):42-4. PubMed ID: 3487275
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Brief cytogenetic case report: a 4.5-year-old girl with deletion 4q syndrome--de novo, 46,XX, del(4) (pter leads to q31:).
    Young RS; Palmer CG; Bender HA; Weaver DD; Hodes ME
    Am J Med Genet; 1982 May; 12(1):103-7. PubMed ID: 7091193
    [No Abstract]   [Full Text] [Related]  

  • 9. Mapping of genes encoding coagulation factors VII and X to the distal portion of the 13q34 by gene dose study in a patient with r(13).
    Kasai R; Narahara K; Namba H; Tsuji K; Matsubara T; Hiramoto K; Yokoyama Y; Kimoto H
    Jinrui Idengaku Zasshi; 1989 Sep; 34(3):247-50. PubMed ID: 2634139
    [No Abstract]   [Full Text] [Related]  

  • 10. Severe FX deficiency caused by a previously unidentified 4-bp deletion compound heterozygous with a large deletion involving FVII and FX genes.
    Tan CW; Najm J; Morel-Kopp MC; Teo J; Chen Q; Felbor U; Ward CM
    Haemophilia; 2012 Mar; 18(2):e55-8. PubMed ID: 22126652
    [No Abstract]   [Full Text] [Related]  

  • 11. Evidence that activities of coagulation factors VII and X are linked to chromosome 13 (q34).
    Ott R; Pfeiffer RA
    Hum Hered; 1984; 34(2):123-6. PubMed ID: 6745952
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Deletion 1q42.3----qter in a girl with psychomotoric retardation and multiple dysmorphisms.
    Kausch K; Köhler J; Schmid M
    Ann Genet; 1988; 31(3):193-4. PubMed ID: 3265611
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Boy with celiac disease, malformations, and ring chromosome 13 with deletion 13q32-->qter.
    Talvik I; Ounap K; Bartsch O; Ilus T; Uibo O; Talvik T
    Am J Med Genet; 2000 Aug; 93(5):399-402. PubMed ID: 10951464
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter).
    Syrrou M; Borghgraef M; Fryns JP
    Am J Med Genet; 2001 Dec; 104(3):199-203. PubMed ID: 11754044
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chromosomal arrangement of the murine coagulation factor VII and factor X genes.
    Liang Z; Cooper A; Rosen ED; Castellino FJ
    Thromb Haemost; 1998 Sep; 80(3):524-5. PubMed ID: 9759642
    [No Abstract]   [Full Text] [Related]  

  • 16. Blepharophimosis sequence (BPES) and microcephaly in a girl with del(3) (q22.2q23): a putative gene responsible for microcephaly close to the BPES gene?
    Ishikiriyama S; Goto M
    Am J Med Genet; 1993 Sep; 47(4):487-9. PubMed ID: 8256811
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)].
    Chitayat D; Babul R; Silver MM; Jay V; Teshima IE; Babyn P; Becker LE
    Am J Med Genet; 1996 Jan; 61(1):45-8. PubMed ID: 8741917
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Complex chromosome rearrangements and congenital anomalies.
    Kousseff BG; Nichols P; Essig YP; Miller K; Weiss A; Tedesco TA
    Am J Med Genet; 1987 Apr; 26(4):771-82. PubMed ID: 3591822
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A malformed girl with a de novo proximal 6q deletion.
    Lonardo F; Colantuoni M; Festa B; Gentile G; Guerritore G; Perone L; Santulli B; Ventruto V
    Ann Genet; 1988; 31(1):57-9. PubMed ID: 3281572
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 4.