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 *

139 related articles for article (PubMed ID: 17194334)

  • 1. [De novo partial monosomy 10p].
    Ibáñez Micó S; Solaz Barrios S; Aleu Pérez-Gramunt M; García Vicent C
    An Pediatr (Barc); 2006 Dec; 65(6):627-8. PubMed ID: 17194334
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. [Monosomy 7qter (author's transl)].
    Turleau C; de Grouchy J; Perignon F; Lenoir G
    Ann Genet; 1979; 22(4):242-4. PubMed ID: 317790
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ophthalmic findings in partial monosomy 4p (Wolf syndrome) in combination with partial trisomy 10p.
    Seiberth V; Kachel W; Knorz MC; Liesenhoff H
    Am J Ophthalmol; 1994 Mar; 117(3):411-3. PubMed ID: 8129026
    [No Abstract]   [Full Text] [Related]  

  • 5. Family with partial monosomy 10p and trisomy 10p.
    Hon E; Chapman C; Gunn TR
    Am J Med Genet; 1995 Mar; 56(2):136-40. PubMed ID: 7625434
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. A case of de novo translocation 7; 10 and the duplication 7p, deletion 10p phenotype.
    Park JP; McDermet MK; Moeschler JB; Wurster-Hill DH
    Ann Genet; 1993; 36(4):217-20. PubMed ID: 8166428
    [TBL] [Abstract][Full Text] [Related]  

  • 8. De novo 10q22 interstitial deletion.
    Cook L; Weaver DD; Hartsfield JK; Vance GH
    J Med Genet; 1999 Jan; 36(1):71-2. PubMed ID: 9950372
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [A case of 9p partial monosomy syndrome].
    Zhang JH; Qiao NN; Li W; Wang JW
    Zhonghua Er Ke Za Zhi; 2013 Sep; 51(9):697-8. PubMed ID: 24330994
    [No Abstract]   [Full Text] [Related]  

  • 11. Partial monosomy of distal 10q: three new cases and a review.
    Waggoner DJ; Chow CK; Dowton SB; Watson MS
    Am J Med Genet; 1999 Sep; 86(1):1-5. PubMed ID: 10440820
    [TBL] [Abstract][Full Text] [Related]  

  • 12. De novo terminal deletion of chromosome 7 [46,XX,del(7)(q35)].
    Lo BH; Murch A; Chabros V; Withnell R
    J Paediatr Child Health; 1996 Aug; 32(4):347-9. PubMed ID: 8844544
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial monosomy of 7q32 in a case of de novo rcp(7;15)(q32;q15).
    D'Alessandro E; Ligas C; Lo Re ML; Marcanio MP; Gentile T; Del Porto G
    J Med Genet; 1994 May; 31(5):413-5. PubMed ID: 8064823
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Monosomy 16q: a distinct syndrome. Apropos of a de novo del(16) (q2100q2300).
    Rivera H; Vargas-Moyeda E; Möller M; Torres-Lamas A; Cantú JM
    Clin Genet; 1985 Jul; 28(1):84-6. PubMed ID: 4028506
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CATCHing a break on 22.
    Glover TW
    Nat Genet; 1995 Jul; 10(3):257-8. PubMed ID: 7670460
    [No Abstract]   [Full Text] [Related]  

  • 16. 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes.
    Grammatico P; Majore S; Marrocco G; Poscente M; Mordenti C; Grammatico B; Del Porto G
    Genet Couns; 1999; 10(4):351-8. PubMed ID: 10631922
    [TBL] [Abstract][Full Text] [Related]  

  • 17. MRI findings in a patient with partial monosomy 10p.
    Sunada F; Rash FC; Tam DA
    J Med Genet; 1998 Feb; 35(2):159-61. PubMed ID: 9507399
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Possible isochromosome 22 leading to trisomy 22.
    Manasse BF; Pfaffenzeller WM; Gurtunca N; de Ravel TJ
    Am J Med Genet; 2000 Dec; 95(5):411-4. PubMed ID: 11146458
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Wolf-Hirschorn syndrome resulting from partial monosomy 4p/trisomy 9p.
    Xu J; Freeman V; Carter RF; Paes B; Heshka T; Nowaczyk JM
    Am J Med Genet; 2000 Aug; 93(4):285-9. PubMed ID: 10946354
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A case of ring chromosome 2 with growth retardation, mild dysmorphism, and microdeletion of 2p detected using FISH.
    Dee SL; Clark AT; Willatt LR; Yates JR
    J Med Genet; 2001 Sep; 38(9):E32. PubMed ID: 11546833
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.