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 *

161 related articles for article (PubMed ID: 18412119)

  • 21. Deletion of 4.4 Mb at 2q33.2q33.3 May Cause Growth Deficiency in a Patient with Mental Retardation, Facial Dysmorphic Features and Speech Delay.
    Papoulidis I; Paspaliaris V; Papageorgiou E; Siomou E; Dagklis T; Sotiriou S; Thomaidis L; Manolakos E
    Cytogenet Genome Res; 2015; 145(1):19-24. PubMed ID: 25925190
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 12q12 deletion: a new patient contributing to genotype-phenotype correlation.
    Failla P; Romano C; Reitano S; Di Benedetto D; Grillo L; Fichera M; Castiglia L
    Am J Med Genet A; 2008 May; 146A(10):1354-7. PubMed ID: 18412123
    [No Abstract]   [Full Text] [Related]  

  • 23. A 797 kb de novo deletion of 18q21.31 in a patient with speech delay, mental retardation, sleeping problems, facial dysmorphism, and feet anomalies.
    van Diepen MM; Gijsbers AC; Bosch CA; Oudesluys-Murphy AM; Ruivenkamp CA; Bijlsma EK
    Eur J Med Genet; 2011; 54(1):86-8. PubMed ID: 20870045
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mother to son transmission of del(1) (q42.1q42.3).
    Sanford Hanna JA; Ball S; Pagon RA; Donlan M
    Am J Med Genet; 2001 Jan; 98(1):103-6. PubMed ID: 11426447
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Proximal interstitial 1p36 deletion syndrome: the most proximal 3.5-Mb microdeletion identified on a dysmorphic and mentally retarded patient with inv(3)(p14.1q26.2).
    Shimojima K; Páez MT; Kurosawa K; Yamamoto T
    Brain Dev; 2009 Sep; 31(8):629-33. PubMed ID: 18835671
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Association between deletion size and important phenotypes expands the genomic region of interest in Phelan-McDermid syndrome (22q13 deletion syndrome).
    Sarasua SM; Dwivedi A; Boccuto L; Rollins JD; Chen CF; Rogers RC; Phelan K; DuPont BR; Collins JS
    J Med Genet; 2011 Nov; 48(11):761-6. PubMed ID: 21984749
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Novel duplication on chromosome 16 (q12.1-q21) associated with behavioral disorder, mild cognitive impairment, speech delay, and dysmorphic features: case report.
    Odak L; Barisić I; Morozin Pohovski L; Riegel M; Schinzel A
    Croat Med J; 2011 Jun; 52(3):415-22. PubMed ID: 21674840
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Deletion of chromosome region 18q21.1 --> 18q21.3 in a patient without clinical features of the 18q- phenotype.
    Engelen JJ; Moog U; Weber J; Haagen AA; van Uum CM; Hamers AJ
    Am J Med Genet A; 2003 Jun; 119A(3):356-9. PubMed ID: 12784305
    [TBL] [Abstract][Full Text] [Related]  

  • 29. High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype.
    Callen DF; Eyre H; Lane S; Shen Y; Hansmann I; Spinner N; Zackai E; McDonald-McGinn D; Schuffenhauer S; Wauters J
    J Med Genet; 1993 Oct; 30(10):828-32. PubMed ID: 8230159
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Loss of the N-myc oncogene in a patient with a small interstitial deletion of the short arm of chromosome 2.
    Saal HM; King LJ; Zimmerman D; Johnson RC; Carr AG; Samango-Sprouse CA; Stanley W
    Am J Med Genet; 1996 Dec; 66(4):373-7. PubMed ID: 8989454
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Multigeneration family with short stature, developmental delay, and dysmorphic features due to 4q27-q28.1 microdeletion.
    Hickey SE; Biswas S; Thrush DL; Pyatt RE; Gastier-Foster JM; Astbury C; Atkin J
    Eur J Med Genet; 2013 Sep; 56(9):521-5. PubMed ID: 23895773
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Further delineation of the 22q13 deletion syndrome.
    Lindquist SG; Kirchhoff M; Lundsteen C; Pedersen W; Erichsen G; Kristensen K; Lillquist K; Smedegaard HH; Skov L; Tommerup N; Brøndum-Nielsen K
    Clin Dysmorphol; 2005 Apr; 14(2):55-60. PubMed ID: 15770125
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Polycystic kidneys and del (4)(q21.1q21.3): further delineation of a distinct phenotype.
    Velinov M; Kupferman J; Gu H; Macera MJ; Babu A; Jenkins EC; Kupchik G
    Eur J Med Genet; 2005; 48(1):51-5. PubMed ID: 15953406
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Molecular cytogenetic analysis of a de novo interstitial chromosome 10q22 deletion.
    Tzschach A; Krause-Plonka I; Menzel C; Knoblauch A; Toennies H; Hoeltzenbein M; Radke M; Ropers HH; Kalscheuer V
    Am J Med Genet A; 2006 May; 140(10):1108-10. PubMed ID: 16619204
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Interstitial deletion of chromosome 12q: genotype-phenotype correlation of two patients utilizing array comparative genomic hybridization.
    Klein OD; Cotter PD; Schmidt AM; Bick DP; Tidyman WE; Albertson DG; Pinkel D; Rauen KA
    Am J Med Genet A; 2005 Nov; 138(4):349-54. PubMed ID: 16200635
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Interstitial deletion of the long arm of chromosome 8. Karyotype: 46,XY,del(8)(q21).
    Fryns JP; Logghe N; Van Eygen M; Van Der Berghe H
    Hum Genet; 1979 Apr; 48(1):127-30. PubMed ID: 457127
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech.
    Bonnet C; Andrieux J; Béri-Dexheimer M; Leheup B; Boute O; Manouvrier S; Delobel B; Copin H; Receveur A; Mathieu M; Thiriez G; Le Caignec C; David A; de Blois MC; Malan V; Philippe A; Cormier-Daire V; Colleaux L; Flori E; Dollfus H; Pelletier V; Thauvin-Robinet C; Masurel-Paulet A; Faivre L; Tardieu M; Bahi-Buisson N; Callier P; Mugneret F; Edery P; Jonveaux P; Sanlaville D
    J Med Genet; 2010 Jun; 47(6):377-84. PubMed ID: 20522426
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Interstitial 6q deletion: clinical and array CGH characterisation of a new patient.
    Le Caignec C; Swillen A; Van Asche E; Fryns JP; Vermeesch JR
    Eur J Med Genet; 2005; 48(3):339-45. PubMed ID: 16179229
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34.3 microdeletions.
    Willemsen MH; Beunders G; Callaghan M; de Leeuw N; Nillesen WM; Yntema HG; van Hagen JM; Nieuwint AW; Morrison N; Keijzers-Vloet ST; Hoischen A; Brunner HG; Tolmie J; Kleefstra T
    Clin Genet; 2011 Jul; 80(1):31-8. PubMed ID: 21204793
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Subtelomeric 6.7 Mb trisomy 10p and 5.6 Mb monosomy 21q detected by FISH and array-CGH in three related patients.
    Szabó GP; Knegt AC; Ujfalusi A; Balogh E; Szabó T; Oláh É
    Am J Med Genet A; 2012 Apr; 158A(4):869-76. PubMed ID: 22407767
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.