BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

593 related articles for article (PubMed ID: 15181786)

  • 21. Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size.
    Shinawi M; Liu P; Kang SH; Shen J; Belmont JW; Scott DA; Probst FJ; Craigen WJ; Graham BH; Pursley A; Clark G; Lee J; Proud M; Stocco A; Rodriguez DL; Kozel BA; Sparagana S; Roeder ER; McGrew SG; Kurczynski TW; Allison LJ; Amato S; Savage S; Patel A; Stankiewicz P; Beaudet AL; Cheung SW; Lupski JR
    J Med Genet; 2010 May; 47(5):332-41. PubMed ID: 19914906
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications.
    Swillen A; Vogels A; Devriendt K; Fryns JP
    Am J Med Genet; 2000; 97(2):128-35. PubMed ID: 11180220
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Velo-cardio-facial syndrome, schizophrenia and deletion at chromosome 22q11.
    Chow LY; Waye MM; Garcia-Barcelo M; Chiu HF; Fung KP; Lee CY
    J Intellect Disabil Res; 1998 Apr; 42 ( Pt 2)():184-8. PubMed ID: 9617702
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 19q13.32 microdeletion syndrome: three new cases.
    Castillo A; Kramer N; Schwartz CE; Miles JH; DuPont BR; Rosenfeld JA; Graham JM
    Eur J Med Genet; 2014; 57(11-12):654-8. PubMed ID: 25230004
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Cerebral polymicrogyria and 22q11 deletion syndrome].
    Arriola-Pereda G; Verdú-Pérez A; de Castro-De Castro P
    Rev Neurol; 2009 Feb 16-28; 48(4):188-90. PubMed ID: 19226486
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome.
    Lachman HM; Morrow B; Shprintzen R; Veit S; Parsia SS; Faedda G; Goldberg R; Kucherlapati R; Papolos DF
    Am J Med Genet; 1996 Sep; 67(5):468-72. PubMed ID: 8886163
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders.
    Carlson C; Papolos D; Pandita RK; Faedda GL; Veit S; Goldberg R; Shprintzen R; Kucherlapati R; Morrow B
    Am J Hum Genet; 1997 Apr; 60(4):851-9. PubMed ID: 9106531
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [The 22q11.2 deletion syndrome: immunological questions].
    Paśnik J; Cywińska-Bernas A; Piotrowicz M
    Postepy Hig Med Dosw (Online); 2007 Jun; 61():361-8. PubMed ID: 17572656
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The Danish 22q11 research initiative.
    Schmock H; Vangkilde A; Larsen KM; Fischer E; Birknow MR; Jepsen JR; Olesen C; Skovby F; Plessen KJ; Mørup M; Hulme O; Baaré WF; Didriksen M; Siebner HR; Werge T; Olsen L
    BMC Psychiatry; 2015 Sep; 15():220. PubMed ID: 26384214
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations.
    Ravnan JB; Chen E; Golabi M; Lebo RV
    Am J Med Genet; 1996 Dec; 66(3):250-6. PubMed ID: 8985481
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Developmental trajectories in 22q11.2 deletion.
    Swillen A; McDonald-McGinn D
    Am J Med Genet C Semin Med Genet; 2015 Jun; 169(2):172-81. PubMed ID: 25989227
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [A bifid uvula in a patient with schizophrenia as a sign of 22q11 deletion syndrome].
    Vorstman JA; de Ranitz AG; Udink ten Cate FE; Beemer FA; Kahn RS
    Ned Tijdschr Geneeskd; 2002 Oct; 146(43):2033-6. PubMed ID: 12428463
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Chromosome 22q11 deletion and other chromosome aberrations in cases with cleft palate, congenital heart defects and/or mental disability. A survey based on the Danish Facial Cleft Register.
    Brøndum-Nielsen K; Christensen K
    Clin Genet; 1996 Sep; 50(3):116-20. PubMed ID: 8946108
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Behavior and corpus callosum morphology relationships in velocardiofacial syndrome (22q11.2 deletion syndrome).
    Antshel KM; Conchelos J; Lanzetta G; Fremont W; Kates WR
    Psychiatry Res; 2005 Apr; 138(3):235-45. PubMed ID: 15854791
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Velocardiofacial syndrome in childhood-onset schizophrenia.
    Usiskin SI; Nicolson R; Krasnewich DM; Yan W; Lenane M; Wudarsky M; Hamburger SD; Rapoport JL
    J Am Acad Child Adolesc Psychiatry; 1999 Dec; 38(12):1536-43. PubMed ID: 10596254
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions.
    Lindsay EA; Goldberg R; Jurecic V; Morrow B; Carlson C; Kucherlapati RS; Shprintzen RJ; Baldini A
    Am J Med Genet; 1995 Jul; 57(3):514-22. PubMed ID: 7677167
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1.
    Rajcan-Separovic E; Harvard C; Liu X; McGillivray B; Hall JG; Qiao Y; Hurlburt J; Hildebrand J; Mickelson EC; Holden JJ; Lewis ME
    J Med Genet; 2007 Apr; 44(4):269-76. PubMed ID: 16963482
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Syndromes 3. Velo-cardio-facial (VCF/Shprintzen) syndrome].
    Beemer FA
    Ned Tijdschr Tandheelkd; 1998 Aug; 105(8):287-8. PubMed ID: 11928434
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Annotation: velo-cardio-facial syndrome.
    Murphy KC
    J Child Psychol Psychiatry; 2005 Jun; 46(6):563-71. PubMed ID: 15877762
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Screening of patients at risk for 22q11 deletion.
    Barisić I; Morozin Pohovski L; Petković I; Cvetko Z; Stipancić G; Bagatin M
    Coll Antropol; 2008 Mar; 32(1):165-9. PubMed ID: 18494202
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 30.