165 related articles for article (PubMed ID: 33292381)
1. A rare cardiac phenotype of dextrocardia observed in a fetus with 1p36 deletion syndrome and a balanced translocation: a prenatal case report.
Gao L; Zhang J; Han X; Hu W; Sun J; Tan Y; Zhao X; Hua R; Wang S; Zhang Y; Wang Y; Wu Y
Mol Cytogenet; 2020 Nov; 13(1):48. PubMed ID: 33292381
[TBL] [Abstract][Full Text] [Related]
2. Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome.
Toshimitsu M; Nagaoka S; Kobori S; Ogawa M; Suzuki F; Kato T; Miyai S; Kawamura R; Inagaki H; Kurahashi H; Murotsuki J
Case Rep Obstet Gynecol; 2019; 2019():6753184. PubMed ID: 31662930
[TBL] [Abstract][Full Text] [Related]
3. Genetic Analysis of 1p36 Deletions for Six Aborted Fetuses.
Shen Y; Zhang W; Hua P; Qian F
Altern Ther Health Med; 2024 Feb; ():. PubMed ID: 38401069
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis of pure 1p36 terminal deletion by chromosome microarry analysis - clinical report of 3 new cases and review of the literature.
Song T; Zheng J; Li Y; Li J; Guo F; Zhao S; Zhang W; Xu Y; Yang H
Ginekol Pol; 2022 Jan; ():. PubMed ID: 35072240
[TBL] [Abstract][Full Text] [Related]
5. Prenatal detection of 1p36 deletion syndrome: ultrasound findings and microarray testing results.
Zhang X; He P; Han J; Pan M; Yang X; Zhen L; Liao C; Li DZ
J Matern Fetal Neonatal Med; 2021 Jul; 34(13):2180-2184. PubMed ID: 31446820
[TBL] [Abstract][Full Text] [Related]
6. Array-based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardation.
Lennon PA; Cooper ML; Curtis MA; Lim C; Ou Z; Patel A; Cheung SW; Bacino CA
Am J Med Genet A; 2006 Jun; 140(11):1156-63. PubMed ID: 16688748
[TBL] [Abstract][Full Text] [Related]
7. Prenatal findings in 1p36 deletion syndrome: New cases and a literature review.
Guterman S; Beneteau C; Redon S; Dupont C; Missirian C; Jaeger P; Herve B; Jacquin C; Douet-Guilbert N; Till M; Tabet AC; Moradkhani K; Malan V; Doco-Fenzy M; Vialard F
Prenat Diagn; 2019 Sep; 39(10):871-882. PubMed ID: 31172545
[TBL] [Abstract][Full Text] [Related]
8. Dextrocardia, atrial septal defect, severe developmental delay, facial anomalies, and supernumerary ribs in a child with a complex unbalanced 8;22 translocation including partial 8p duplication.
Pope K; Samanich J; Ramesh KH; Cannizzaro L; Pan Q; Babcock M
Am J Med Genet A; 2012 Mar; 158A(3):641-7. PubMed ID: 22302699
[TBL] [Abstract][Full Text] [Related]
9. Array comparative genomic hybridisation-based identification of two imbalances of chromosome 1p in a 9-year-old girl with a monosomy 1p36 related phenotype and a family history of learning difficulties: a case report.
Fitzgibbon GJ; Clayton-Smith J; Banka S; Hamilton SJ; Needham MM; Dore JK; Miller JT; Pawson GD; Gaunt L
J Med Case Rep; 2008 Nov; 2():355. PubMed ID: 19019217
[TBL] [Abstract][Full Text] [Related]
10. Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: a case report.
Nistico' D; Guidolin F; Navarra CO; Bobbo M; Magnolato A; D'Adamo AP; Giorgio E; Pivetta B; Barbi E; Gasparini P; Cadenaro M; Sirchia F
BMC Pediatr; 2020 May; 20(1):201. PubMed ID: 32386509
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of monosomy 1p36: a focus on brain abnormalities and a review of the literature.
Campeau PM; Ah Mew N; Cartier L; Mackay KL; Shaffer LG; Der Kaloustian VM; Thomas MA
Am J Med Genet A; 2008 Dec; 146A(23):3062-9. PubMed ID: 19006213
[TBL] [Abstract][Full Text] [Related]
12. Deletion in 1p36.33-p36.32 is associated with pancytopenia: a case report.
Yang H; Huang J; Zheng H; Zhang Y; Zhang Y; Liu W; Wu J; Chen X; Lin J; Ni Y; Nie X
BMC Med Genomics; 2023 Nov; 16(1):282. PubMed ID: 37946214
[TBL] [Abstract][Full Text] [Related]
13. Epilepsy and neurological findings in 11 individuals with 1p36 deletion syndrome.
Kurosawa K; Kawame H; Okamoto N; Ochiai Y; Akatsuka A; Kobayashi M; Shimohira M; Mizuno S; Wada K; Fukushima Y; Kawawaki H; Yamamoto T; Masuno M; Imaizumi K; Kuroki Y
Brain Dev; 2005 Aug; 27(5):378-82. PubMed ID: 16023556
[TBL] [Abstract][Full Text] [Related]
14. Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
Chen CP; Chen M; Su YN; Hsu CY; Tsai FJ; Chern SR; Wu PC; Lee CC; Wang W
Taiwan J Obstet Gynecol; 2010 Dec; 49(4):473-80. PubMed ID: 21199750
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis.
Mademont-Soler I; Morales C; Soler A; Martínez-Crespo JM; Shen Y; Margarit E; Clusellas N; Obón M; Wu BL; Sánchez A
Ultrasound Obstet Gynecol; 2013 Apr; 41(4):375-82. PubMed ID: 23233332
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Prenatal diagnosis of a fetus affected with Down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping.
Hsieh LJ; Hsieh TC; Yeh GP; Lin MI; Chen M; Wang BB
Fetal Diagn Ther; 2004; 19(4):356-60. PubMed ID: 15192296
[TBL] [Abstract][Full Text] [Related]
18. [Prenatal diagnosis of two fetuses with chromosome 1p36 deletion syndrome].
Ji X; Hu H; Wang Y; Liang D; Luo C; Meng L; Zhou J; Cao L; Ma D; Hu P; Xu Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Dec; 34(6):853-856. PubMed ID: 29188615
[TBL] [Abstract][Full Text] [Related]
19. Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review.
Yokoyama E; Villarroel CE; Diaz S; Del Castillo V; Pérez-Vera P; Salas C; Gómez S; Barreda R; Molina B; Frias S
Mol Cytogenet; 2020; 13():42. PubMed ID: 32939224
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]