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 *

115 related articles for article (PubMed ID: 35666339)

  • 61. Genomic imbalances in craniofacial microsomia.
    Spineli-Silva S; Sgardioli IC; Dos Santos AP; Bergamini LL; Monlleó IL; Fontes MIB; Félix TM; Ribeiro EM; Xavier AC; Lustosa-Mendes E; Gil-da-Silva-Lopes VL; Vieira TP
    Am J Med Genet C Semin Med Genet; 2020 Dec; 184(4):970-985. PubMed ID: 33215817
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Copy number variations in multicystic dysplastic kidney: update for prenatal diagnosis and genetic counseling.
    Xi Q; Zhu X; Wang Y; Ru T; Dai C; Wang Z; Li J; Hu Y
    Prenat Diagn; 2016 May; 36(5):463-8. PubMed ID: 26941192
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Contribution of genomic copy-number variations in prenatal oral clefts: a multicenter cohort study.
    Cao Y; Li Z; Rosenfeld JA; Pursley AN; Patel A; Huang J; Wang H; Chen M; Sun X; Leung TY; Cheung SW; Choy KW
    Genet Med; 2016 Oct; 18(10):1052-5. PubMed ID: 26913922
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Characterization of Copy-Number Variations and Possible Candidate Genes in Recurrent Pregnancy Losses.
    Sheng YR; Hou SY; Hu WT; Wei CY; Liu YK; Liu YY; Jiang L; Xiang JJ; Sun XX; Lei CX; Wang HL; Zhu XY
    Genes (Basel); 2021 Jan; 12(2):. PubMed ID: 33499090
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Genomic imbalances in the placenta are associated with poor fetal growth.
    Del Gobbo GF; Yin Y; Choufani S; Butcher EA; Wei J; Rajcan-Separovic E; Bos H; von Dadelszen P; Weksberg R; Robinson WP; Yuen RKC
    Mol Med; 2021 Jan; 27(1):3. PubMed ID: 33413077
    [TBL] [Abstract][Full Text] [Related]  

  • 66. New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.
    Cappuccio G; Vitiello F; Casertano A; Fontana P; Genesio R; Bruzzese D; Ginocchio VM; Mormile A; Nitsch L; Andria G; Melis D
    Ital J Pediatr; 2016 Apr; 42():39. PubMed ID: 27072107
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Why do euploid embryos miscarry? A case-control study comparing the rate of aneuploidy within presumed euploid embryos that resulted in miscarriage or live birth using next-generation sequencing.
    Maxwell SM; Colls P; Hodes-Wertz B; McCulloh DH; McCaffrey C; Wells D; Munné S; Grifo JA
    Fertil Steril; 2016 Nov; 106(6):1414-1419.e5. PubMed ID: 27692437
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Estimation on risk of spontaneous abortions by genomic disorders from a meta-analysis of microarray results on large case series of pregnancy losses.
    Peng G; Zhou Q; Chai H; Wen J; Zhao H; Taylor HS; Jiang YH; Li P
    Mol Genet Genomic Med; 2023 Aug; 11(8):e2181. PubMed ID: 37013615
    [TBL] [Abstract][Full Text] [Related]  

  • 69. [CNV-seq analysis of copy number variations in 217 fetuses with nasal bone dysplasia].
    Shi P; Hou Y; Chen D; Liu N; Jiao Z; Feng Y; Sun G; Zhu R; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Oct; 39(10):1076-1079. PubMed ID: 36184086
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Identification of genomic imbalances (CNVs as well as LOH) in sertoli cell only syndrome cases through cytoscan microarray.
    Sharma A; Jain M; Halder A; Kaushal S
    Gene; 2021 Oct; 801():145851. PubMed ID: 34274474
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Clinical utility of expanded non-invasive prenatal screening compared with chromosomal microarray analysis in over 8000 pregnancies without major structural anomaly.
    Maya I; Salzer Sheelo L; Brabbing-Goldstein D; Matar R; Kahana S; Agmon-Fishman I; Klein C; Gurevitch M; Basel-Salmon L; Sagi-Dain L
    Ultrasound Obstet Gynecol; 2023 Jun; 61(6):698-704. PubMed ID: 36776119
    [TBL] [Abstract][Full Text] [Related]  

  • 72. [Correlation of fetal ventriculomegaly with copy number variations and pregnancy outcome].
    Gao C; Dou J; Yang S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Dec; 38(12):1254-1257. PubMed ID: 34839519
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Chromosomal microarray analysis of infertile men with azoospermia factor microdeletions.
    Zhu Y; Hu L; Cao D; Ou X; Jiang M
    Gene; 2020 Apr; 735():144389. PubMed ID: 31982552
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Clinical application of SNP array analysis in first-trimester pregnancy loss: a prospective study.
    Wang Y; Cheng Q; Meng L; Luo C; Hu H; Zhang J; Cheng J; Xu T; Jiang T; Liang D; Hu P; Xu Z
    Clin Genet; 2017 Jun; 91(6):849-858. PubMed ID: 27883173
    [TBL] [Abstract][Full Text] [Related]  

  • 75. [Comprehensive genetic analysis in first or second trimester pregnancy loss using chromosomal microarray with single nucleotide polymorphism probes].
    Zhu L; Zhang H; Du Q; Sun X; Liu W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Jun; 39(6):576-580. PubMed ID: 35773758
    [TBL] [Abstract][Full Text] [Related]  

  • 76. [Application of next generation sequencing for the detection of chromosomal aneuploidies and copy number variations in abortus tissues].
    Chen J; Hu L; Yang J; Liu P
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Aug; 35(4):591-594. PubMed ID: 30098263
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders.
    Akter H; Rahman MM; Sarker S; Basiruzzaman M; Islam MM; Rahaman MA; Rahaman MA; Eshaque TB; Dity NJ; Sarker S; Amin MR; Hossain MM; Lopa M; Jahan N; Hossain S; Islam A; Mondol A; Faruk MO; Saha N; Kundu GK; Kanta SI; Kazal RK; Fatema K; Rahman MA; Hasan M; Hossain Mollah MA; Hosen MI; Karuvantevida N; Begum G; Zehra B; Nassir N; Nabi AHMN; Uddin KMF; Uddin M
    Front Genet; 2023; 14():955631. PubMed ID: 36959829
    [No Abstract]   [Full Text] [Related]  

  • 78. Effects of platforms, size filter cutoffs, and targeted regions of cytogenomic microarray on detection of copy number variants and uniparental disomy in prenatal diagnosis: Results from 5026 pregnancies.
    Wang JC; Radcliff J; Coe SJ; Mahon LW
    Prenat Diagn; 2019 Feb; 39(3):137-156. PubMed ID: 30734327
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability.
    Borlot F; Regan BM; Bassett AS; Stavropoulos DJ; Andrade DM
    JAMA Neurol; 2017 Nov; 74(11):1301-1311. PubMed ID: 28846756
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Exome sequencing as first-tier test for fetuses with severe central nervous system structural anomalies.
    Yaron Y; Ofen Glassner V; Mory A; Zunz Henig N; Kurolap A; Bar Shira A; Brabbing Goldstein D; Marom D; Ben Sira L; Baris Feldman H; Malinger G; Krajden Haratz K; Reches A
    Ultrasound Obstet Gynecol; 2022 Jul; 60(1):59-67. PubMed ID: 35229910
    [TBL] [Abstract][Full Text] [Related]  

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