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 *

152 related articles for article (PubMed ID: 38250576)

  • 1. Variable clinical presentation of split hand/foot malformation syndrome in a family with microduplication of 10q24.32: a case report.
    Akimova D; Markova T; Ampleeva M; Skoblov M
    Front Genet; 2023; 14():1303807. PubMed ID: 38250576
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Microduplication of BTRC detected in a Chinese family with split hand/foot malformation type 3.
    Qiu L; Li C; Zheng G; Yang T; Yang F
    Clin Genet; 2022 Nov; 102(5):451-456. PubMed ID: 35908152
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular Genetic Characterization of a Chinese Family with Severe Split Hand/Foot Malformation.
    Cao L; Yang W; Wang S; Chen C; Zhang X; Luo Y
    Genet Test Mol Biomarkers; 2017 Jun; 21(6):357-362. PubMed ID: 28422522
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Somatic/gonadal mosaicism in a syndromic form of ectrodactyly, including eye abnormalities, documented through array-based comparative genomic hybridization.
    Filho AB; Souza J; Faucz FR; Sotomaior VS; Dupont B; Bartel F; Rodriguez R; Schwartz CE; Skinner C; Alliman S; Raskin S
    Am J Med Genet A; 2011 May; 155A(5):1152-6. PubMed ID: 21485001
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Discontinuous microduplications at chromosome 10q24.31 identified in a Chinese family with split hand and foot malformation.
    Dai L; Deng Y; Li N; Xie L; Mao M; Zhu J
    BMC Med Genet; 2013 Apr; 14():45. PubMed ID: 23596994
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Microduplications of 10q24 Detected in Two Chinese Patients with Split-hand/foot Malformation Type 3.
    Xiang R; Du R; Guo S; Jin JY; Fan LL; Tang JY; Zhou ZB
    Ann Clin Lab Sci; 2017 Nov; 47(6):754-757. PubMed ID: 29263051
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of Critical Region Responsible for Split Hand/Foot Malformation Type 3 (SHFM3) Phenotype through Systematic Review of Literature and Mapping of Breakpoints Using Microarray Data.
    Li CF; Angione K; Milunsky JM
    Microarrays (Basel); 2015 Dec; 5(1):. PubMed ID: 27600068
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Genetic analysis of a pedigree affected with congenital split-hand/foot malformation].
    Li Q; Tong M; Chen C; Ji Y; Zhou K; Xu G; Hu S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Apr; 37(4):467-470. PubMed ID: 32219839
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genomic rearrangement at 10q24 in non-syndromic split-hand/split-foot malformation.
    Kano H; Kurosawa K; Horii E; Ikegawa S; Yoshikawa H; Kurahashi H; Toda T
    Hum Genet; 2005 Dec; 118(3-4):477-83. PubMed ID: 16235095
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation.
    Everman DB; Morgan CT; Lyle R; Laughridge ME; Bamshad MJ; Clarkson KB; Colby R; Gurrieri F; Innes AM; Roberson J; Schrander-Stumpel C; van Bokhoven H; Antonarakis SE; Schwartz CE
    Am J Med Genet A; 2006 Jul; 140(13):1375-83. PubMed ID: 16761290
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Distal limb deficiencies, micrognathia syndrome, and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangements.
    Dimitrov BI; de Ravel T; Van Driessche J; de Die-Smulders C; Toutain A; Vermeesch JR; Fryns JP; Devriendt K; Debeer P
    J Med Genet; 2010 Feb; 47(2):103-11. PubMed ID: 19584065
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An Unusual Presentation of Bilateral Split Hand-Foot Malformation (SHFM) in Family: A Tale of Two Generations.
    Singh SV; Puri G; Gemmy AE
    Curr Health Sci J; 2022; 48(3):356-359. PubMed ID: 36815080
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 17p13.3 genomic rearrangement in a Chinese family with split-hand/foot malformation with long bone deficiency: report of a complicated duplication with marked variation in phenotype.
    Shen Y; Si N; Liu Z; Liu F; Meng X; Zhang Y; Zhang X
    Orphanet J Rare Dis; 2018 Jul; 13(1):106. PubMed ID: 29970136
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Split-hand/foot malformation 3 resulting from microduplications in 10q24 region in five patients from India.
    Langeh N; Ansari MT; Kabra M; Gupta N
    Am J Med Genet A; 2024 May; 194(5):e63520. PubMed ID: 38168117
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Split hand/foot malformation with long bone deficiency associated with BHLHA9 gene duplication: a case report and review of literature.
    Paththinige CS; Sirisena ND; Escande F; Manouvrier S; Petit F; Dissanayake VHW
    BMC Med Genet; 2019 Jun; 20(1):108. PubMed ID: 31200655
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A DNA duplication at chromosome 10q24.3 is associated with split-hand split-foot malformation in a Chinese family].
    Yang W; Hu ZJ; Yu XF; Li QH; Zhang AJ; Deng X; Zhang AY; Gao CS; Liu Y; Ao Y; Lo WH; Zhang X
    Zhonghua Yi Xue Za Zhi; 2006 Mar; 86(10):652-8. PubMed ID: 16681918
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Genetic analysis of a Chinese pedigree affected with congenital split-hand/foot malformation].
    Mei L; He X; Gao H; Huang Y; Wu X; He H; Li P
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Dec; 38(12):1208-1210. PubMed ID: 34839508
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Congenital ectrodactyly caused by chromosome 10q24.31 duplication and its pathogenetic analysis].
    Zhang XQ; Wang J; Xiong F; Lv WB; Zhou YQ; Yang SM; Zhang YT; Tian XY; Lian W; Xu XM
    Yi Chuan; 2019 Aug; 41(8):716-724. PubMed ID: 31447422
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Identification of a pathogenic microduplication in a Chinese split-hand/split-foot malformation family].
    Liu Y; Huang Y; Yang W; Zhang X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun; 31(3):276-9. PubMed ID: 24928001
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 7q21.3 Deletion involving enhancer sequences within the gene DYNC1I1 presents with intellectual disability and split hand-split foot malformation with decreased penetrance.
    Delgado S; Velinov M
    Mol Cytogenet; 2015; 8():37. PubMed ID: 26075025
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.