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 *

164 related articles for article (PubMed ID: 11565549)

  • 21. Duplication 20p identified via fluorescent in situ hybridization.
    LeChien KA; McPherson E; Estop AM
    Am J Med Genet; 1994 Apr; 50(2):187-9. PubMed ID: 7516625
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Two supernumerary marker chromosomes, originating from chromosomes 6 and 11, in a child with developmental delay and craniofacial dysmorphism.
    Maurer B; Haaf T; Stout K; Reissmann N; Steinlein C; Schmid M
    Cytogenet Cell Genet; 2001; 93(3-4):182-7. PubMed ID: 11528110
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Developmental delay and dysmorphic features associated with a previously undescribed deletion on chromosome 1.
    Barton JS; O'Loughlin J; Howell RT; L'e Orme R
    J Med Genet; 1995 Aug; 32(8):636-7. PubMed ID: 7473657
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Cytogenetic and array-CGH characterization of a 6q27 deletion in a patient with developmental delay and features of Ehlers-Danlos syndrome.
    Mosca AL; Callier P; Masurel-Paulet A; Thauvin-Robinet C; Marle N; Nouchy M; Huet F; Dipanda D; De Paepe A; Coucke P; Mugneret F; Faivre L
    Am J Med Genet A; 2010 May; 152A(5):1314-7. PubMed ID: 20425843
    [No Abstract]   [Full Text] [Related]  

  • 25. Interstitial deletion of the long arm of chromosome 11: report of a case and review of the literature.
    Wakazono A; Masuno M; Yamaguchi S; Tsubouchi K; Kondo N; Orii T
    Jpn J Hum Genet; 1992 Sep; 37(3):229-34. PubMed ID: 1472705
    [TBL] [Abstract][Full Text] [Related]  

  • 26. De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder.
    Goumy C; Mihaescu M; Tchirkov A; Giollant M; Benier C; Francannet C; Jaffray JY; Geneix A; Vago P
    Genet Couns; 2006; 17(3):371-9. PubMed ID: 17100206
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Incidental finding of paternal UPD15 in a child with a deletion of 11q21-q22.3, presenting with developmental delay, coloboma and characteristic dysmorphic features.
    Tucker T; Steinraths M; Oh T; Nelson TN; Van Allen MI; Brown L; Schlade-Bartusiak K
    Clin Dysmorphol; 2016 Apr; 25(2):77-81. PubMed ID: 26636500
    [No Abstract]   [Full Text] [Related]  

  • 28. An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.
    Bremer A; Schoumans J; Nordenskjöld M; Anderlid BM; Giacobini M
    Eur J Med Genet; 2009; 52(5):358-62. PubMed ID: 19576304
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A case with 47,XXY,del(11)(q23) karotype-coexistence of Jacobsen and Klinefelter syndromes.
    Matheisel A; Babinska M; Wierzba J; Wozniak A; Nedoszytko B; Balcerska A; Limon J
    Genet Couns; 2000; 11(3):267-71. PubMed ID: 11043435
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Novel case of del(17)(q23.1q23.3) further highlights a recognizable phenotype involving deletions of chromosome (17)(q21q24).
    Mickelson EC; Robinson WP; Hrynchak MA; Lewis ME
    Am J Med Genet; 1997 Aug; 71(3):275-9. PubMed ID: 9268095
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A case with de novo interstitial deletion of chromosome 7q21.1-q22.
    Manguoğlu E; Berker-Karaüzüm S; Baumer A; Mihçi E; Taçoy S; Lüleci G; Schinzel A
    Genet Couns; 2005; 16(2):155-9. PubMed ID: 16080295
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 18q- and 18q+ mosaicism in a mentally retarded boy.
    Ausems MG; Bhola SL; Post-Blok CA; Hennekam RC; de France HF
    Am J Med Genet; 1994 Nov; 53(3):296-9. PubMed ID: 7856666
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Familial (11;21)(p13;q22)pat balanced reciprocal translocation in a female child with regression of milestones.
    Ramadevi AR; Prabhakara K; Dutta U
    Ann Genet; 2002; 45(1):13-5. PubMed ID: 11934384
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Identification of the chromosome 14 origin of a C-negative marker associated with a 14q32 deletion by chromosome painting.
    Magnani I; Sacchi N; Darfler M; Nisson PE; Tornaghi R; Fuhrman-Conti AM
    Clin Genet; 1993 Apr; 43(4):180-5. PubMed ID: 7687207
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 11p14.1 microdeletions associated with ADHD, autism, developmental delay, and obesity.
    Shinawi M; Sahoo T; Maranda B; Skinner SA; Skinner C; Chinault C; Zascavage R; Peters SU; Patel A; Stevenson RE; Beaudet AL
    Am J Med Genet A; 2011 Jun; 155A(6):1272-80. PubMed ID: 21567907
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Interstitial deletion of chromosome 18[del(18)(q11.2q12.2 or q12.2q21.1].
    Surh LC; Ledbetter DH; Greenberg F
    Am J Med Genet; 1991 Oct; 41(1):15-7. PubMed ID: 1719812
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion.
    Lefort G; Blanchet P; Belgrade N; Rivier F; Chaze AM; Sarda P; Demaille J; Pellestor F
    Am J Med Genet A; 2003 Apr; 118A(2):333-8. PubMed ID: 12698965
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Identification of supernumerary marker chromosomes derived from chromosomes 5, 6, 19, and 20 using FISH.
    Stankiewicz P; Bocian E; Jakubów-Durska K; Obersztyn E; Lato E; Starke H; Mroczek K; Mazurczak T
    J Med Genet; 2000 Feb; 37(2):114-20. PubMed ID: 10662811
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Congenital indifference to pain and deletion of chromosome 10q-: new association.
    Joshi C; Dawson AJ; Sanders SR; Prasad C
    J Child Neurol; 2006 Feb; 21(2):174-7. PubMed ID: 16566889
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Interstitial deletion of the long arm of chromosome 11 determined by fluorescence in situ hybridization.
    Hori T; Masuno M; Wakazono A; Takahashi E; Katakura R; Orii T
    Jpn J Hum Genet; 1993 Jun; 38(2):219-24. PubMed ID: 8358045
    [TBL] [Abstract][Full Text] [Related]  

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