BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 33429816)

  • 1. Prenatal detection of a 3q29 microdeletion in a fetus with ventricular septum defect: A case report and literature review.
    Yue F; Deng S; Xi Q; Jiang Y; He J; Zhang H; Liu R
    Medicine (Baltimore); 2021 Jan; 100(1):e24224. PubMed ID: 33429816
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal detection of distal 1q21.1q21.2 microduplication with abnormal ultrasound findings: Two cases report and literature review.
    Zhang H; Yue F; Zhang X; He J; Jiang Y; Liu R; Yu Y
    Medicine (Baltimore); 2021 Jan; 100(1):e24227. PubMed ID: 33429818
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 15q24 microdeletion.
    Chen CP; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2020 May; 59(3):432-436. PubMed ID: 32416893
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial inheritance of the 3q29 microdeletion syndrome: case report and review.
    Khan WA; Cohen N; Scott SA; Pereira EM
    BMC Med Genomics; 2019 Mar; 12(1):51. PubMed ID: 30885185
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A clinical case report and literature review of the 3q29 microdeletion syndrome.
    Cox DM; Butler MG
    Clin Dysmorphol; 2015 Jul; 24(3):89-94. PubMed ID: 25714563
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis of a de novo 15q11.2 microdeletion in a maternal inv(4)(p15q31) fetus with increased nuchal translucency: A case report and literature review.
    Sun M; Yue F; Yu Y; Li L; Jiang Y; Zhang H; Liu R
    Medicine (Baltimore); 2020 Oct; 99(40):e22496. PubMed ID: 33019446
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 3q29 microdeletion syndrome associated with developmental delay and pulmonary stenosis: a case report.
    Kaba D; Çelik ZY
    Turk J Pediatr; 2022; 64(5):925-931. PubMed ID: 36305444
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound.
    Chen CP; Chang SY; Wang LK; Chang TY; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Town DD; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2018 Oct; 57(5):730-733. PubMed ID: 30342661
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound.
    Chen CP; Chang SY; Lin CJ; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Chen WL; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2018 Oct; 57(5):734-738. PubMed ID: 30342662
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical application of SNP array analysis in fetuses with ventricular septal defects and normal karyotypes.
    Fu F; Deng Q; Lei TY; Li R; Jing XY; Yang X; Liao C
    Arch Gynecol Obstet; 2017 Nov; 296(5):929-940. PubMed ID: 28905115
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Detection of recurrent 4p16.3 microdeletion with 2p25.3 microduplication by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in a fetus from a family with Wolf-Hirschhorn syndrome.
    Yang WX; Pan H; Wang ST; Li L; Wu HR; Qi Y
    Taiwan J Obstet Gynecol; 2016 Feb; 55(1):104-8. PubMed ID: 26927259
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular cytogenetic characterization of a de novo chromosome 1q41-q42.11 microdeletion of paternal origin in a 15-year-old boy with mental retardation, developmental delay, autism and congenital heart defects.
    Chen CP; Chern SR; Wu PS; Chen SW; Wu FT; Wang W
    Taiwan J Obstet Gynecol; 2021 Mar; 60(2):341-344. PubMed ID: 33678339
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical, cytogenetic, and molecular findings in a fetus with ultrasonic multiple malformations, 4q duplication, and 7q deletion: A case report and literature review.
    Yue F; Jiang Y; Yu Y; Yang X; Zhang H; Liu R; Wang R
    Medicine (Baltimore); 2018 Nov; 97(45):e13094. PubMed ID: 30407316
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defects.
    Chen CP; Chen CY; Chern SR; Wu PS; Chen SW; Wu FT; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2019 Sep; 58(5):704-708. PubMed ID: 31542097
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1, NIPA2, CYFIP1, and TUBGCP5 associated with phenotypic variability in developmental, speech, and motor delay.
    Chen CP; Lin SP; Lee CL; Chern SR; Wu PS; Chen YN; Chen SW; Wang W
    Taiwan J Obstet Gynecol; 2017 Feb; 56(1):93-97. PubMed ID: 28254235
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 1.6Mb deletion in chromosome band 3q29 associated with eye abnormalities.
    Tyshchenko N; Hackmann K; Gerlach EM; Neuhann T; Schrock E; Tinschert S
    Eur J Med Genet; 2009; 52(2-3):128-30. PubMed ID: 19298871
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Genetic analysis of two fetuses with congenital heart defects and 3q microdeletion].
    Long W; Gu J; Ouyang J; Jia S; Zhang B; Liu J; Yu B
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr; 35(2):240-243. PubMed ID: 29653001
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Molecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes].
    Quintela I; Barros-Angueira F; Perez-Gay L; Dacruz D; Castro-Gago M; Carracedo A; Eiris-Punal J
    Rev Neurol; 2015 Sep; 61(6):255-60. PubMed ID: 26350776
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 1q42.3-q44 deletion in a fetus associated with ventriculomegaly on prenatal ultrasound.
    Chen CP; Ko TM; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2020 Jul; 59(4):598-603. PubMed ID: 32653137
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Paroxysmal oculogyric dystonia associated with a de novo 3q29 microdeletion.
    Kaur H; Thom RP; Neumeyer AM; Bilancia CG; Wray SH; McDougle CJ
    Psychiatr Genet; 2020 Aug; 30(4):119-123. PubMed ID: 32459710
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.