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 *

70 related articles for article (PubMed ID: 9489800)

  • 1. Deletion 8p syndrome.
    Digilio MC; Marino B; Guccione P; Giannotti A; Mingarelli R; Dallapiccola B
    Am J Med Genet; 1998 Feb; 75(5):534-6. PubMed ID: 9489800
    [No Abstract]   [Full Text] [Related]  

  • 2. Interstitial deletion of chromosome 5 in a neonate due to maternal insertion, ins(8;5)(p23;q33q35).
    Gibbons B; Tan SY; Kee SK; Quaife R; Lim ST
    Am J Med Genet; 1999 Sep; 86(3):289-93. PubMed ID: 10482883
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: relevance to ocular dysgenesis and hearing impairment.
    Gould DB; Jaafar MS; Addison MK; Munier F; Ritch R; MacDonald IM; Walter MA
    BMC Med Genet; 2004 Jun; 5():17. PubMed ID: 15219231
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Lobar holoprosencephaly in 18pter deletion resulting from the karyotype 45,X,-18,der(8;18)t(8; 18)(pter;p11.21).
    Witters I; Balikova I; Cannie M; Devriendt K; De Catte L; Fryns JP
    Genet Couns; 2008; 19(4):443-6. PubMed ID: 19239091
    [No Abstract]   [Full Text] [Related]  

  • 5. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
    Karmous-Benailly H; Giuliano F; Massol C; Bloch C; De Ricaud D; Lambert JC; Perelman S
    Eur J Med Genet; 2006; 49(5):431-8. PubMed ID: 16497571
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A re-examination of the chromosome 8p22-8p23.1 region in Kabuki syndrome.
    Milunsky JM; Maher TA; Zhao G; Huang XL; Wang Z; Zou Y
    Clin Genet; 2008 May; 73(5):502-3. PubMed ID: 18336587
    [No Abstract]   [Full Text] [Related]  

  • 7. Velocardiofacial syndrome (Shprintzen syndrome, chromosome 22q11 deletion syndrome).
    Olney AH; Kolodziej P
    Ear Nose Throat J; 1998 Jun; 77(6):460-1. PubMed ID: 9674319
    [No Abstract]   [Full Text] [Related]  

  • 8. Molecular cytogenetic analysis of de novo partial monosomy 4p (4p16.2-->pter) and partial trisomy 8p (8p23.2-->pter).
    Chen CP; Lin SP; Chern SR; Lee CC; Chen LF; Chen YJ; Wang W
    Genet Couns; 2006; 17(1):81-5. PubMed ID: 16719283
    [No Abstract]   [Full Text] [Related]  

  • 9. Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion.
    Wuyts W; Roland D; Lüdecke HJ; Wauters J; Foulon M; Van Hul W; Van Maldergem L
    Am J Med Genet; 2002 Dec; 113(4):326-32. PubMed ID: 12457403
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Two adjacent microdeletions in 8q11.2 cause a phenotype suggestive of the 22q11 deletion syndrome.
    Ockeloen CW; de Leeuw N; Mieloo H; Reijnen IGM; de Vries BBA
    Clin Dysmorphol; 2010 Jul; 19(3):137-139. PubMed ID: 20357662
    [No Abstract]   [Full Text] [Related]  

  • 12. Wolf-Hirschhorn(4p-) syndrome.
    Mathai S; Ganguly BB
    Indian Pediatr; 2003 Jul; 40(7):681. PubMed ID: 12881629
    [No Abstract]   [Full Text] [Related]  

  • 13. Fetoplacental discrepancy involving structural abnormalities of chromosome 8 detected by prenatal diagnosis.
    Soler A; Sánchez A; Carrió A; Badenas C; Milà M; Borrell A
    Prenat Diagn; 2003 Apr; 23(4):319-22. PubMed ID: 12673638
    [TBL] [Abstract][Full Text] [Related]  

  • 14. New case of contiguous gene syndrome at chromosome 8p11.2p12.
    Cau M; Congiu R; Origa R; Galanello R; Melis MA; Nucaro AL
    Am J Med Genet A; 2005 Jul; 136(2):221-2. PubMed ID: 15948194
    [No Abstract]   [Full Text] [Related]  

  • 15. Anaesthesia in a child with deletion 13q syndrome.
    Inada T; Matsumoto H; Shingu K
    Paediatr Anaesth; 1998; 8(5):441. PubMed ID: 9742544
    [No Abstract]   [Full Text] [Related]  

  • 16. Smith-Magenis syndrome and tetralogy of Fallot.
    Sweeney E; Peart I; Tofeig M; Kerr B
    J Med Genet; 1999 Jun; 36(6):501-2. PubMed ID: 10874646
    [No Abstract]   [Full Text] [Related]  

  • 17. De-novo interstitial 2.33 Mb deletion in 8q24.3: new insights on a very rare partial monosomy syndrome.
    Akbaroghli S; Tonekaboni SH; Kariminejad R; Liehr T; Coci EG
    Clin Dysmorphol; 2018 Jul; 27(3):97-100. PubMed ID: 29738340
    [No Abstract]   [Full Text] [Related]  

  • 18. Preaxial polydactyly in the 4p- syndrome.
    Schrander-Stumpel CT; Rijnvos WP; van der Blij-Philipsen M; Drogtrop A; Smeets D; Fryns JP
    Genet Couns; 1998; 9(1):63-5. PubMed ID: 9555593
    [No Abstract]   [Full Text] [Related]  

  • 19. Unilateral Peters' anomaly in an infant with 22q11.2 deletion syndrome.
    Erdoğan MK; Utine GE; Alanay Y; Aktaş D
    Clin Dysmorphol; 2008 Oct; 17(4):289-90. PubMed ID: 18978663
    [No Abstract]   [Full Text] [Related]  

  • 20. Mosaic supernumerary r(8) syndrome.
    Yilmaz S; Tarkan-Argüden Y; Kuru D; Deviren A; Karaman B; Yüksel A; Hacihanefioğlu S
    Genet Couns; 2005; 16(2):187-90. PubMed ID: 16080301
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.