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 *

121 related articles for article (PubMed ID: 21910236)

  • 1. Inherited interstitial 16q21 deletion of 5.8 Mb without apparent phenotypic effect in three generations of a family: an array-CGH study.
    Coussement A; Lochu P; Dupont JM; Choiset A
    Am J Med Genet A; 2011 Oct; 155A(10):2597-600. PubMed ID: 21910236
    [No Abstract]   [Full Text] [Related]  

  • 2. A familial deletion of 16q21 characterized by an SNP array and associated with a normal phenotype.
    Kowalczyk M; Tomaszewska A; Podbiol-Palenta A; Remiszewska B; Galjaard RJ; Zajaczek S; Srebniak MI
    Am J Med Genet A; 2013 Jun; 161A(6):1501-4. PubMed ID: 23633153
    [No Abstract]   [Full Text] [Related]  

  • 3. Clinical report: AN INTERSTITIAL deletion of 16p13.11 detected by array CGH in a patient with infantile spasms.
    Balasubramanian M; Smith K; Mordekar SR; Parker MJ
    Eur J Med Genet; 2011; 54(3):314-8. PubMed ID: 21315189
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Interstitial deletion of 6q without phenotypic effect.
    Hansson K; Szuhai K; Knijnenburg J; van Haeringen A; de Pater J
    Am J Med Genet A; 2007 Jun; 143A(12):1354-7. PubMed ID: 17506100
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An unusual chromosome 22q11 deletion associated with an apparent complementary ring chromosome in a phenotypically normal woman.
    Toutain J; Taine L; Morice-Picard F; Hallal H; Dai ZQ; Arveiler B; Lacombe D; Horovitz J; Saura R
    Eur J Med Genet; 2011; 54(3):292-4. PubMed ID: 21215339
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial 14.5 Mb interstitial deletion 13q21.1-13q21.33: clinical and array-CGH study of a benign phenotype in a three-generation family.
    Filges I; Röthlisberger B; Noppen C; Boesch N; Wenzel F; Necker J; Binkert F; Huber AR; Heinimann K; Miny P
    Am J Med Genet A; 2009 Feb; 149A(2):237-41. PubMed ID: 19161139
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Haploinsufficiency and triploinsensitivity of the same 6p25.1p24.3 region in a family.
    Qi Z; Jeng LJ; Slavotinek A; Yu J
    BMC Med Genomics; 2015 Jul; 8():38. PubMed ID: 26174853
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome.
    Koczkowska M; Wierzba J; Śmigiel R; Sąsiadek M; Cabała M; Ślężak R; Iliszko M; Kardaś I; Limon J; Lipska-Ziętkiewicz BS
    J Appl Genet; 2017 Feb; 58(1):93-98. PubMed ID: 27629806
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial 4.8 MB deletion on 18q23 associated with growth hormone insufficiency and phenotypic variability.
    Margarit E; Morales C; Rodríguez-Revenga L; Monné R; Badenas C; Soler A; Clusellas N; Mademont I; Sánchez A
    Am J Med Genet A; 2012 Mar; 158A(3):611-6. PubMed ID: 22302430
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inherited interstitial deletion of chromosomes 5p and 16q without apparent phenotypic effect: further confirmation.
    Hand JL; Michels VV; Marinello MJ; Ketterling RP; Jalal SM
    Prenat Diagn; 2000 Feb; 20(2):144-8; discussion 149-51. PubMed ID: 10694687
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Co-existence of 9p deletion and Silver-Russell syndromes in a patient with maternally inherited cryptic complex chromosome rearrangement involving chromosomes 4, 9, and 11.
    Hu J; Sathanoori M; Kochmar S; Madan-Khetarpal S; McGuire M; Surti U
    Am J Med Genet A; 2013 Jan; 161A(1):179-84. PubMed ID: 23225375
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Array-CGH revealed one of the smallest 16q21q22.1 microdeletions in a female patient with psychomotor retardation.
    Tsoutsou E; Tzetis M; Giannikou K; Syrmou A; Oikonomakis V; Kosma K; Kanioura A; Kanavakis E; Fryssira H
    Eur J Paediatr Neurol; 2013 May; 17(3):316-20. PubMed ID: 23352671
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of a 12q22q23.2 interstitial deletion by array CGH in a malformed fetus.
    Kremer V; Girard F; Gasser B; Marcellin L; Christmann D; Nisand I; Schmitt E; Florent S; Flori E
    Eur J Med Genet; 2012 Apr; 55(4):269-73. PubMed ID: 22425634
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A 2 Mb deletion in 14q13 associated with severe developmental delay and hemophagocytic lymphohistiocytosis.
    Caliebe A; Martin Subero JI; Muhle H; Gesk S; Jänig U; Krause M; Plendl H; Stephani U; Siebert R; Eckmann-Scholz C
    Eur J Med Genet; 2011; 54(5):e505-9. PubMed ID: 21736959
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Duplication 16q12.1-q22.1 characterized by array CGH in a girl with spina bifida.
    Gustavsson P; Schoumans J; Staaf J; Borg A; Nordenskjöld M; Annerén G
    Eur J Med Genet; 2007; 50(3):237-41. PubMed ID: 17387046
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Interstitial deletion at chromosome 16p13.2 involving TMEM114 (transmembrane protein 114) in a boy and his father without cataract.
    Gai D; Nicholl J; Waters W; Barnett CP; Yu S
    Am J Med Genet A; 2014 Mar; 164A(3):834-6. PubMed ID: 24357539
    [No Abstract]   [Full Text] [Related]  

  • 17. Developmental delay and facial dysmorphism in a child with an 8.9 Mb de novo interstitial deletion of 3q25.1-q25.32: Genotype-phenotype correlations of chromosome 3q25 deletion syndrome.
    Moortgat S; Verellen-Dumoulin C; Maystadt I; Parmentier B; Grisart B; Hennecker JL; Destree A
    Eur J Med Genet; 2011; 54(2):177-80. PubMed ID: 21167329
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Identification of a novel deletion region in 3q29 microdeletion syndrome by oligonucleotide array comparative genomic hybridization].
    Seo EJ; Jun KR; Yoo HW; Yoo HK; Lee JO
    Korean J Lab Med; 2010 Feb; 30(1):70-5. PubMed ID: 20197726
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [One case of 2q37 deletion syndrome: clinical and genetic diagnosis].
    Geng Q; Xie JS; Wu WQ; Luo FW; Chen WB
    Zhonghua Er Ke Za Zhi; 2013 Dec; 51(12):934-7. PubMed ID: 24495766
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An additional case of the recurrent 15q24.1 microdeletion syndrome and review of the literature.
    L Ng IS; Chin WH; P Lim EC; Tan EC
    Twin Res Hum Genet; 2011 Aug; 14(4):333-9. PubMed ID: 21787116
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.