141 related articles for article (PubMed ID: 36544198)
1. Prenatal diagnosis and molecular cytogenetic analyses of a paternal inherited deletion of 1q23.3 encompassing PBX1 gene.
Luo M; Gu X; Zhou T; Chen C
Mol Cytogenet; 2022 Dec; 15(1):53. PubMed ID: 36544198
[TBL] [Abstract][Full Text] [Related]
2. Prenatal findings and molecular cytogenetic analyses of a de novo interstitial deletion of 1q23.3 encompassing PBX1 gene.
Sun M; Lou J; Li Q; Chen J; Li Y; Li D; Yuan H; Liu Y
Taiwan J Obstet Gynecol; 2019 Mar; 58(2):292-295. PubMed ID: 30910156
[TBL] [Abstract][Full Text] [Related]
3. 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]
4.
Le Tanno P; Breton J; Bidart M; Satre V; Harbuz R; Ray PF; Bosson C; Dieterich K; Jaillard S; Odent S; Poke G; Beddow R; Digilio MC; Novelli A; Bernardini L; Pisanti MA; Mackenroth L; Hackmann K; Vogel I; Christensen R; Fokstuen S; Béna F; Amblard F; Devillard F; Vieville G; Apostolou A; Jouk PS; Guebre-Egziabher F; Sartelet H; Coutton C
J Med Genet; 2017 Jul; 54(7):502-510. PubMed ID: 28270404
[TBL] [Abstract][Full Text] [Related]
5. Case Report: Candidate Genes Associated With Prenatal Ultrasound Anomalies in a Fetus With Prenatally Detected 1q23.3q31.2 Deletion.
Song J; Zhang Q; Lu B; Gou Z; Wang T; Tang H; Xiang J; Jiang W; Deng X
Front Genet; 2021; 12():696624. PubMed ID: 34630509
[No Abstract] [Full Text] [Related]
6. Prenatal Diagnosis and Molecular Cytogenetic Analyses of a de novo Deletion on Chromosome 4p16.3p15.33.
Luo H; Chang R; Liu F; Gao X
Altern Ther Health Med; 2023 Nov; 29(8):907-909. PubMed ID: 37708564
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis and genetic counseling of an inherited unbalanced chromosome abnormalities in a Chinese family.
Zhang Y; Chen J; Feng Z; Li W
Mol Cytogenet; 2022 Aug; 15(1):34. PubMed ID: 35971114
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis and genetic counseling of a uniparental isodisomy of chromosome 8 with no phenotypic abnormalities.
Yu C; Tian Y; Qi L; Wang B
Mol Cytogenet; 2022 Apr; 15(1):18. PubMed ID: 35473567
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Prenatal diagnosis and genetic counseling of an inherited Xq24q25 deletion associated with normal phenotype.
Zhou Y; Zhang M; Zhu Y; Zhao Q
Mol Cytogenet; 2022 Nov; 15(1):49. PubMed ID: 36329552
[TBL] [Abstract][Full Text] [Related]
11. Identification of a Novel Heterozygous
Riedhammer KM; Siegel C; Alhaddad B; Montoya C; Kovacs-Nagy R; Wagner M; Meitinger T; Hoefele J
Front Pediatr; 2017; 5():251. PubMed ID: 29226118
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Whole-exome sequencing for prenatal diagnosis of fetuses with congenital anomalies of the kidney and urinary tract.
Lei TY; Fu F; Li R; Wang D; Wang RY; Jing XY; Deng Q; Li ZZ; Liu ZQ; Yang X; Li DZ; Liao C
Nephrol Dial Transplant; 2017 Oct; 32(10):1665-1675. PubMed ID: 28387813
[TBL] [Abstract][Full Text] [Related]
16. Molecular cytogenetic characterization of 2q deletion and Xq duplication associated with nasal bone dysplasia in prenatal diagnosis: A case report and literature review.
Sun ML; Yue FG; Zhang XY; Jiang YT; Li LL; Zhang HG; Liu RZ
Taiwan J Obstet Gynecol; 2022 Jan; 61(1):163-169. PubMed ID: 35181032
[TBL] [Abstract][Full Text] [Related]
17. Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1-related syndrome.
Arts P; Garland J; Byrne AB; Hardy TSE; Babic M; Feng J; Wang P; Ha T; King-Smith SL; Schreiber AW; Crawford A; Manton N; Moore L; Barnett CP; Scott HS
Am J Med Genet A; 2020 May; 182(5):1273-1277. PubMed ID: 32141698
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.
Chen CP; Su YN; Chen YY; Su JW; Chern SR; Chen YT; Chen WL; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):506-11. PubMed ID: 22212326
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis and molecular cytogenetic characterization of a de novo 3.19-Mb chromosome 14q32.13-q32.2 deletion of paternal origin.
Chen CP; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Chen WL; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2020 Sep; 59(5):766-769. PubMed ID: 32917334
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]