BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

52 related articles for article (PubMed ID: 22086126)

  • 1. 7q31.32 partial duplication: First report of a child with dysmorphism, autistic spectrum disorder, moderate intellectual disability and, epilepsy. Literature review.
    Pavone P; Corsello G; Marino SD; Ruggieri M; Falsaperla R
    Epilepsy Res; 2019 Dec; 158():106223. PubMed ID: 31707317
    [TBL] [Abstract][Full Text] [Related]  

  • 2. De novo dup(7)(q21q22.2) and cytogenetics of 7q21q34 duplications.
    Rivera H
    Genet Couns; 2013; 24(3):291-7. PubMed ID: 24341144
    [TBL] [Abstract][Full Text] [Related]  

  • 3. De novo duplication and deletions at 7q in a three-generation family.
    Isidor B; Villa O; Pichon O; Briand A; Poulain D; Boisseau P; Pérez-Jurado LA; Le Caignec C
    Am J Med Genet A; 2012 Jun; 158A(6):1493-7. PubMed ID: 22577094
    [No Abstract]   [Full Text] [Related]  

  • 4. A 0.7 Mb de novo duplication at 7q21.3 including the genes DLX5 and DLX6 in a patient with split-hand/split-foot malformation.
    Velinov M; Ahmad A; Brown-Kipphut B; Shafiq M; Blau J; Cooma R; Roth P; Iqbal MA
    Am J Med Genet A; 2012 Dec; 158A(12):3201-6. PubMed ID: 23169702
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genomic Complexity and Complex Chromosomal Rearrangements in Genetic Diagnosis: Two Illustrative Cases on Chromosome 7.
    Villa N; Redaelli S; Farina S; Conconi D; Sala EM; Crosti F; Mariani S; Colombo CM; Dalprà L; Lavitrano M; Bentivegna A; Roversi G
    Genes (Basel); 2023 Aug; 14(9):. PubMed ID: 37761840
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pure Interstitial 7q21.3-q 31.1 Duplication: A Rare Segmental Genomic Aneuploidy: Case Report and Review of Cases with Distal and Similar Segment Involved.
    Di Nora A; Lena G; Giugno A; Di Mari A; Smilari P; Minardi C; Pavone P
    Glob Med Genet; 2021 Sep; 8(3):123-128. PubMed ID: 34430965
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pure Distal 7q Duplication: Describing a Macrocephalic Neurodevelopmental Syndrome, Case Report and Review of the Literature.
    Bosfield K; Diaz J; Leon E
    Mol Syndromol; 2021 Jun; 12(3):159-168. PubMed ID: 34177432
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 4q27 deletion and 7q36.1 microduplication in a patient with multiple malformations and hearing loss: a case report.
    Wu M; Zheng X; Wang X; Zhang G; Kuang J
    BMC Med Genomics; 2020 Mar; 13(1):31. PubMed ID: 32126996
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal identification of two discontinuous maternally inherited chromosome 7q36.3 microduplications totaling 507 kb including the sonic hedgehog gene in a fetus with multiple congenital anomalies.
    Micale M; Embrey B; Hubbell K; Beaudry-Rogers K; Whitten A
    Clin Case Rep; 2017 Jun; 5(6):993-999. PubMed ID: 28588853
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deletion 21q22.3 and duplication 7q35q36.3 in a Colombian girl: a case report.
    Ruiz-Botero F; Pachajoa H
    J Med Case Rep; 2016 Jul; 10():204. PubMed ID: 27459995
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genomic characterization of some Iranian children with idiopathic mental retardation using array comparative genomic hybridization.
    Behjati F; Firouzabadi SG; Kariminejad R; Vameghi R; Sajedi F; Shafaghati Y; Ghasemlou BE; Shojaei A; Jamali P; Bahman I; Najmabadi H
    Indian J Hum Genet; 2013 Oct; 19(4):443-8. PubMed ID: 24497710
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A new case of pure partial 7q duplication.
    Alfonsi M; Palka C; Morizio E; Gatta V; Franchi S; Guanciali Franchi P; Zori R; Calabrese G; Palka G; Chiarelli F
    Cytogenet Genome Res; 2012; 136(1):1-5. PubMed ID: 22086126
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial trisomy of 7q: case report and literature review.
    Scelsa B; Bedeschi FM; Guerneri S; Lalatta F; Introvini P
    J Child Neurol; 2008 May; 23(5):572-9. PubMed ID: 18056692
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A family with an inverted tandem duplication 5q22.1q23.2.
    Schmidt T; Bartels I; Liehr T; Burfeind P; Zoll B; Shoukier M
    Cytogenet Genome Res; 2013; 139(1):65-70. PubMed ID: 23051634
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A case with partial trisomy 7 (q34→qter) derived from a paternal reciprocal translocation t(7;14)(q34;q32)].
    Xiao B; Ji X; Jiang WT; Zhang JM; Hu Q; Tao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):654-7. PubMed ID: 22161098
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Combined Dup(7)(q22.1q32.2), Inv(7)(q31.31q31.33), and Ins(7;19)(q22.1;p13.2p13.2) in a 12-year-old boy with developmental delay and various dysmorphism.
    Frühmesser A; Erdel M; Duba HC; Fauth C; Amberger A; Utermann G; Zschocke J; Kotzot D
    Eur J Med Genet; 2013 Jul; 56(7):383-8. PubMed ID: 23608969
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Complex rearrangement involving 9p deletion and duplication in a syndromic patient: genotype/phenotype correlation and review of the literature.
    Recalcati MP; Bellini M; Norsa L; Ballarati L; Caselli R; Russo S; Larizza L; Giardino D
    Gene; 2012 Jul; 502(1):40-5. PubMed ID: 22537675
    [TBL] [Abstract][Full Text] [Related]  

  • 18.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.