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 *

252 related articles for article (PubMed ID: 35808818)

  • 1. Prenatal diagnosis and molecular cytogenetic characterization of an inherited microdeletion of chromosome 16p11.2.
    Li M; Liu L; Wu Y; Guan J
    J Int Med Res; 2022 Jul; 50(7):3000605221109400. PubMed ID: 35808818
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and Genetic Study of Three Inherited Microdeletions of Chromosome 16p11.2.
    Liu F; Liu R; Yu C; Duan J; Hu Y; Luo L
    Altern Ther Health Med; 2024 Mar; 30(3):190-192. PubMed ID: 37856819
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal phenotypes and pregnancy outcomes of fetuses with 16p11.2 microdeletion/microduplication.
    Yue F; Hao M; Jiang D; Liu R; Zhang H
    BMC Pregnancy Childbirth; 2024 Jul; 24(1):494. PubMed ID: 39039444
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis and molecular cytogenetic characterization of an inherited microdeletion of 18q12.3 encompassing SETBP1.
    Zhou Y; Quan Y; Wu Y; Zhang Y
    J Int Med Res; 2022 Sep; 50(9):3000605221121955. PubMed ID: 36113068
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Prenatal diagnosis of a fetus with 8q13.3 microdeletion through chromosomal microarray analysis].
    Rao H; Liu Y; Xiao J; Zou Y; Yuan H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Mar; 38(3):268-270. PubMed ID: 33751539
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis by chromosomal microarray analysis.
    Levy B; Wapner R
    Fertil Steril; 2018 Feb; 109(2):201-212. PubMed ID: 29447663
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chromosomal Microarrays for the Prenatal Detection of Microdeletions and Microduplications.
    Wou K; Levy B; Wapner RJ
    Clin Lab Med; 2016 Jun; 36(2):261-76. PubMed ID: 27235911
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Prenatal diagnosis of a fetus with chromosome 18p deletion and duplication].
    Li W; Shao H; Yao J; Shi C; Yang X; Zhang J; Zhang X; Shen G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Jun; 38(6):569-572. PubMed ID: 34096028
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of genetic aberrations in fetuses with pulmonary stenosis in southern China: a retrospective analysis.
    Cai M; Guo N; Fu M; Chen Y; Liang B; Que Y; Ji Q; Huang H; Xu L; Lin N
    BMC Med Genomics; 2023 May; 16(1):119. PubMed ID: 37248535
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular cytogenetic characterization of 16p11.2 microdeletions with diverse prenatal phenotypes: Four cases report and literature review.
    Yue F; Xi Q; Zhang X; Jiang Y; Zhang H; Liu R
    Taiwan J Obstet Gynecol; 2022 May; 61(3):544-550. PubMed ID: 35595456
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal Diagnosis and Molecular Cytogenetic Analyses of a Rare 17q12 Microdeletion and Microduplication in a Family with a Normal Phenotype.
    Xie M; Tang D; Guo F
    Altern Ther Health Med; 2024 Jan; ():. PubMed ID: 38330560
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis and genetic counseling of a paternally inherited chromosome 15q11.2 microdeletion in a Chinese family.
    Tang W; Chen G; Xia J; Zhang Y
    Mol Cytogenet; 2022 Jul; 15(1):28. PubMed ID: 35787815
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Prenatal diagnosis of five fetuses with 7q11.23 microdeletion or microduplication].
    Liang B; Wang Y; Chen L; Huang H; Chen X; He D; Xu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Nov; 38(11):1064-1067. PubMed ID: 34729744
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and genetic study of three families with 15q11q13 duplications.
    Song J; Liu X; Zhang C; Xu F; Wang B
    Taiwan J Obstet Gynecol; 2022 Jul; 61(4):717-721. PubMed ID: 35779929
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Molecular genetic analysis of a child with de novo 16p11.2 microdeletion].
    Zhuang J; Wang Y; Zeng S; Wang J; Jiang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Nov; 37(11):1283-1286. PubMed ID: 33179241
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic effects of a 13q31.1 microdeletion detected by noninvasive prenatal testing (NIPT).
    Jia Y; Zhao H; Shi D; Peng W; Xie L; Wang W; Jiang F; Zhang H; Wang X
    Int J Clin Exp Pathol; 2014; 7(10):7003-11. PubMed ID: 25400788
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic Counseling and Prenatal Diagnosis of a Maternally Inherited 15q11.2 Microduplication.
    Li S; Xie M; Xu E; Zhang Y
    Altern Ther Health Med; 2023 Nov; 29(8):334-336. PubMed ID: 37632958
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal Diagnosis of Chromosome 16p11.2 Microdeletion.
    Wang Y; Zhou H; Fu F; Cheng K; Yu Q; Huang R; Lei T; Yang X; Li D; Liao C
    Genes (Basel); 2022 Dec; 13(12):. PubMed ID: 36553582
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Application of the BACs-on-Beads assay for the prenatal diagnosis of chromosomal abnormalities in Quanzhou, China.
    Zhuang J; Chen C; Jiang Y; Luo Q; Zeng S; Lv C; Wang Y; Fu W
    BMC Pregnancy Childbirth; 2021 Jan; 21(1):94. PubMed ID: 33509128
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pathogenic recurrent copy number variants in 7,078 pregnancies via chromosomal microarray analysis.
    Kang H; Chen Y; Wang L; Gao C; Li X; Hu Y
    J Perinat Med; 2024 Feb; 52(2):171-180. PubMed ID: 38081620
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.