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 *

110 related articles for article (PubMed ID: 31428485)

  • 1. Chromosome 3p Inverted Duplication with Terminal Deletion: Second Postnatal Case Report with Additional Clinical Features.
    Riley JD; Stefaniuk CM; Erenberg F; Erwin AL; Palange L; Astbury C
    Case Rep Genet; 2019; 2019():5384295. PubMed ID: 31428485
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A terminal 3p26.3 deletion is not associated with dysmorphic features and intellectual disability in a four-generation family.
    Moghadasi S; van Haeringen A; Langendonck L; Gijsbers AC; Ruivenkamp CA
    Am J Med Genet A; 2014 Nov; 164A(11):2863-8. PubMed ID: 25123480
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome.
    Cargile CB; Goh DL; Goodman BK; Chen XN; Korenberg JR; Semenza GL; Thomas GH
    Am J Med Genet; 2002 Apr; 109(2):133-8. PubMed ID: 11977162
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A large Indian family with rearrangement of chromosome 4p16 and 3p26.3 and divergent clinical presentations.
    Iype T; Alakbarzade V; Iype M; Singh R; Sreekantan-Nair A; Chioza BA; Mohapatra TM; Baple EL; Patton MA; Warner TT; Proukakis C; Kulkarni A; Crosby AH
    BMC Med Genet; 2015 Nov; 16():104. PubMed ID: 26554554
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inverted duplication deletion of 8P: characterization by standard cytogenetic and SNP array analyses.
    Sireteanu A; Braha E; Popescu R; Gramescu M; Gorduza EV; Rusu C
    Rev Med Chir Soc Med Nat Iasi; 2013; 117(3):731-4. PubMed ID: 24502041
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Detection of a concomitant distal deletion in an inverted duplication of chromosome 3. Is there an overall mechanism for the origin of such duplications/deficiencies?
    Jenderny J; Poetsch M; Hoeltzenbein M; Friedrich U; Jauch A
    Eur J Hum Genet; 1998; 6(5):439-44. PubMed ID: 9801868
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Case Report: A Case Report and Literature Review of 3p Deletion Syndrome.
    Fu J; Wang T; Fu Z; Li T; Zhang X; Zhao J; Yang G
    Front Pediatr; 2021; 9():618059. PubMed ID: 33643973
    [No Abstract]   [Full Text] [Related]  

  • 8. Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature.
    Chen CP; Huang MC; Chern SR; Kuo YL; Chen YN; Wu PS; Chen LF; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2015 Jun; 54(3):297-302. PubMed ID: 26166345
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial monosomy 3p (3p26.2 --> pter) and partial trisomy 5q (5q34 --> qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay.
    Chen CP; Lin SP; Chen MR; Su YN; Chern SR; Liu YP; Su JW; Lee MS; Wang W
    Genet Couns; 2012; 23(3):405-13. PubMed ID: 23072190
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characterization of a complex rearrangement involving duplication and deletion of 9p in an infant with craniofacial dysmorphism and cardiac anomalies.
    Di Bartolo DL; El Naggar M; Owen R; Sahoo T; Gilbert F; Pulijaal VR; Mathew S
    Mol Cytogenet; 2012 Jul; 5(1):31. PubMed ID: 22768875
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Partial trisomy 3p and partial monosomy 11q associated with atrial septal defect, cleft palate, and developmental delay: a case report.
    Tan EC; Lim E; Cham B; Knight L; Ng I
    Cytogenet Genome Res; 2011; 134(4):319-24. PubMed ID: 21654159
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Inverted Duplication and Deletion of 10q25q26 in a Patient without Any Obvious Skeletal Anomalies.
    Xiao B; Ji X; Xing Y; Jiang WT; Zhang JM; Tao J
    Mol Syndromol; 2012 Oct; 3(4):185-9. PubMed ID: 23239961
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A 46,XY Female with a 9p24.3p24.1 Deletion and a 8q24.11q24.3 Duplication: A Case Report and Review of the Literature.
    Bruni V; Roppa K; Scionti F; Apa R; Sestito S; Di Martino MT; Pensabene L; Concolino D
    Cytogenet Genome Res; 2019; 158(2):74-82. PubMed ID: 31141803
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion.
    Knijnenburg J; van Haeringen A; Hansson KB; Lankester A; Smit MJ; Belfroid RD; Bakker E; Rosenberg C; Tanke HJ; Szuhai K
    Eur J Hum Genet; 2007 May; 15(5):548-55. PubMed ID: 17342151
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter).
    Chen CP; Hung FY; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2016 Apr; 55(2):288-92. PubMed ID: 27125417
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Corrigendum to "Chromosome 3p Inverted Duplication with Terminal Deletion: Second Postnatal Case Report with Additional Clinical Features".
    Riley JD; Stefaniuk CM; Erenberg F; Erwin AL; Palange L; Astbury C
    Case Rep Genet; 2019; 2019():4361630. PubMed ID: 31871800
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deletion of chromosome arm 3p in hematologic malignancies.
    Johansson B; Billström R; Kristoffersson U; Akerman M; Garwicz S; Ahlgren T; Malm C; Mitelman F
    Leukemia; 1997 Aug; 11(8):1207-13. PubMed ID: 9264371
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability.
    Ha K; Shen Y; Graves T; Kim CH; Kim HG
    Mol Cytogenet; 2016; 9():74. PubMed ID: 27708714
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An Adolescent with a Rare
    Peterman LA; Vance GH; Conboy EE; Anderson K; Weaver DD
    Case Rep Genet; 2020; 2020():8857628. PubMed ID: 32934853
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.