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 *

109 related articles for article (PubMed ID: 11142759)

  • 61. Interstitial deletion of chromosome 4, del(4)(q12q21.1), in a child with multiple congenital abnormalities.
    Curtis MA; Quarrell OW; Cobon AM; Cummins M
    J Med Genet; 1990 Jan; 27(1):64-5. PubMed ID: 2308158
    [No Abstract]   [Full Text] [Related]  

  • 62. Phenotype-genotype correlation in two patients with 12q proximal deletion.
    Miyake N; Tonoki H; Gallego M; Harada N; Shimokawa O; Yoshiura K; Ohta T; Kishino T; Niikawa N; Matsumoto N
    J Hum Genet; 2004; 49(5):282-4. PubMed ID: 15362574
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Partial deletion of the long arm of chromosome no. 13.
    Cuschieri A; Agius PV; Scheres JM
    Hum Genet; 1977 May; 36(3):341-4. PubMed ID: 852876
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Interstitial deletion of distal 13q associated with Hirschsprung's disease.
    Lamont MA; Fitchett M; Dennis NR
    J Med Genet; 1989 Feb; 26(2):100-4. PubMed ID: 2918536
    [TBL] [Abstract][Full Text] [Related]  

  • 65. De novo deletion 12q: report of a patient with 12q24.31q24.33 deletion.
    Sathya P; Tomkins DJ; Freeman V; Paes B; Nowaczyk MJ
    Am J Med Genet; 1999 May; 84(2):116-9. PubMed ID: 10323735
    [TBL] [Abstract][Full Text] [Related]  

  • 66. A case of Hirschsprung disease with a chromosome 13 microdeletion, del(13)(q32.3q33.2): potential mapping of one disease locus.
    Bottani A; Xie YG; Binkert F; Schinzel A
    Hum Genet; 1991 Oct; 87(6):748-50. PubMed ID: 1937482
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Sperm chromosome analysis to assess potential germ cell mosaicism.
    Brandriff B; Gordon LA; Crawford BB; Schonberg SA; Golabi M; Charzan S; Golbus MS; Carrano AV
    Clin Genet; 1988 Aug; 34(2):85-9. PubMed ID: 3191613
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Craniosynostosis in an infant with an interstitial deletion of 15q [46,XY,del(15)(q15q22.1)].
    Fukushima Y; Wakui K; Nishida T; Nishimoto H
    Am J Med Genet; 1990 Jun; 36(2):209-13. PubMed ID: 2368808
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Deletion of the long arm of chromosome 11: a clinical entity.
    Felding I; Mitelman F
    Acta Paediatr Scand; 1979 Jul; 68(4):635-8. PubMed ID: 463552
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Microdissection-based high-resolution genomic array analysis of two patients with cytogenetically identical interstitial deletions of chromosome 1q but distinct clinical phenotypes.
    Rice GM; Qi Z; Selzer R; Richmond T; Thompson K; Pauli RM; Yu J
    Am J Med Genet A; 2006 Aug; 140(15):1637-43. PubMed ID: 16835927
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Interstitial del(13)(q21.3q31) associated with psychomotor retardation, eczema, and absent suck and swallowing reflex.
    Peet PJ; Pereira RR; Van Hemel JO; Hoogeboom AJ
    J Med Genet; 1987 Dec; 24(12):786-8. PubMed ID: 3430559
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Pseudoachondroplasia with de novo deletion [del(11)(q21q22.2)].
    Ikegawa S; Ohashi H; Hosoda F; Fukushima Y; Ohki M; Nakamura Y
    Am J Med Genet; 1998 Jun; 77(5):356-9. PubMed ID: 9632164
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Terminal deletion of chromosome 1(q43) in a female infant.
    Garani GP; Tamisari L; Volpato S; Vigi V
    J Med Genet; 1988 Mar; 25(3):211-2. PubMed ID: 3351913
    [No Abstract]   [Full Text] [Related]  

  • 74. 13q22.1-q32.1 Microdeletion Syndrome.
    Li MW; Zou XY; Zou CC
    Indian J Pediatr; 2019 Mar; 86(3):303-305. PubMed ID: 30406597
    [No Abstract]   [Full Text] [Related]  

  • 75. [Partial deletion of the short arm of chromosome 13 as an indication of paternity in forensic assessment].
    Gebauer HJ; Scheil HG; Röhrborn G
    Z Rechtsmed; 1988; 99(4):249-51. PubMed ID: 3364043
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Relevance of Fusion Genes in Pediatric Cancers: Toward Precision Medicine.
    Dupain C; Harttrampf AC; Urbinati G; Geoerger B; Massaad-Massade L
    Mol Ther Nucleic Acids; 2017 Mar; 6():315-326. PubMed ID: 28325298
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Characterization of an interstitial deletion del(13)(q22q32) using microdissection and sequential FISH and G-banding.
    Xu J; Chernos JE; Bernier F; Lowry RB
    Genet Test; 2000; 4(3):279-82. PubMed ID: 11142759
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomalies.
    Lorentz CP; Jalal SM; Thompson DM; Babovic-Vuksanovic D
    Am J Med Genet; 2002 Jul; 111(1):61-7. PubMed ID: 12124737
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Interstitial deletion of chromosome 6q: precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting.
    Rubtsov N; Senger G; Kuzcera H; Neumann A; Kelbova C; Junker K; Beensen V; Claussen U
    Hum Genet; 1996 Jun; 97(6):705-9. PubMed ID: 8641683
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
    Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.