Works matching Chromosome abnormalities

Results: 5000

A systematic review and meta-analysis on the association between ICSI and chromosome abnormalities.

Published in:

2021

By:

Berntsen, Sine;
Laivuori, Hannele;
Freiesleben, Nina la Cour;
Loft, Anne;
Söderström-Anttila, Viveca;
Oldereid, Nan B;
Romundstad, Liv Bente;
Magnusson, Åsa;
Petzold, Max;
Bergh, Christina;
Pinborg, Anja;
la Cour Freiesleben, Nina;
B Oldereid, Nan

Publication type:

journal article

Clinical relevance of diagnosing structural chromosome abnormalities in couples with repeated miscarriage.

Published in:

Human Reproduction, 2004, v. 19, n. 4, p. 1013, doi. 10.1093/humrep/deh172

By:

Goddijn, M.;
Joosten, J. H. K.;
Knegt, A. C.;
Van DerVeen, F.;
Franssen, M. T. M.;
Bonsel, G. J.;
Leschot, N. J.

Publication type:

Article

Chromosome Abnormalities and Fertility in Domestic Bovids: A Review.

Published in:

Animals (2076-2615), 2021, v. 11, n. 3, p. 802, doi. 10.3390/ani11030802

By:

Iannuzzi, Alessandra;
Parma, Pietro;
Iannuzzi, Leopoldo;
Lehnert, Sigrid

Publication type:

Article

Relationship between age at menarche and chromosome numerical abnormalities in chorionic villus among missed abortions: A cross‐sectional study of 459 women in China.

Published in:

Journal of Obstetrics & Gynaecology Research, 2020, v. 46, n. 12, p. 2582, doi. 10.1111/jog.14499

By:

Zhao, Lu;
Yang, Hua;
Liu, Guoyan

Publication type:

Article

Reproductive outcomes after preimplantation genetic testing in couples with sex chromosome abnormalities: a retrospective cohort study of 83 couples.

Published in:

Journal of Assisted Reproduction & Genetics, 2024, v. 41, n. 12, p. 3415, doi. 10.1007/s10815-024-03303-6

By:

Yang, Tianying;
Xiao, Min;
Sun, Xiaoxi;
Li, He

Publication type:

Article

Electrofusion Stimulation Is an Independent Factor of Chromosome Abnormality in Mice Oocytes Reconstructed via Spindle Transfer.

Published in:

Frontiers in Endocrinology, 2021, v. 12, p. 1, doi. 10.3389/fendo.2021.705837

By:

Wang, Wei;
Shao, Suxia;
Chen, Wei;
Wang, Weizhou;
Chuai, Yunhai;
Li, Yunfei;
Guo, Yiming;
Han, Shujie;
Shu, Mingming;
Wang, Qihang;
Zhang, Lei;
Shang, Wei

Publication type:

Article

Risk of Chromosome Abnormalities in the Presence of Bilateral or Unilateral Choroid Plexus Cysts.

Published in:

Fetal Diagnosis & Therapy, 2008, v. 23, n. 3, p. 185, doi. 10.1159/000116739

By:

Beke, Artúr;
Barakonyi, Emese;
Belics, Zorán;
Joó, József G.;
Csaba, Ákos;
Papp, Csaba;
Tóth-Pál, Ernő;
Papp, Zoltán

Publication type:

Article

Reproductive outcome after PGD in couples with recurrent miscarriage carrying a structural chromosome abnormality: a systematic review.

Published in:

Human Reproduction Update, 2011, v. 17, n. 4, p. 467, doi. 10.1093/humupd/dmr011

By:

Franssen, M.T.M.;
Musters, A.M.;
van der Veen, F.;
Repping, S.;
Leschot, N.J.;
Bossuyt, P.M.M.;
Goddijn, M.;
Korevaar, J.C.

Publication type:

Article

Increased numbers of DNA-damaged spermatozoa in samples presenting an elevated rate of numerical chromosome abnormalities.

Published in:

Human Reproduction, 2013, v. 28, n. 6, p. 1707, doi. 10.1093/humrep/det077

By:

Enciso, M.;
Alfarawati, S.;
Wells, D.

Publication type:

Article

Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 5, p. 412, doi. 10.1007/s10038-006-0376-7

By:

Miura, Shoko;
Miura, Kiyonori;
Masuzaki, Hideaki;
Miyake, Noriko;
Yoshiura, Koh-ichiro;
Sosonkina, Nadiya;
Harada, Naoki;
Shimokawa, Osamu;
Nakayama, Daisuke;
Yoshimura, Shuichiro;
Matsumoto, Naomichi;
Niikawa, Norio;
Ishimaru, Tadayuki

Publication type:

Article

Chromosomal Abnormalities in Chromosome 5 and Chromosome 8 in Iraqi Patients with Acute Myeloid Leukemia.

Published in:

Iraqi Journal of Cancer & Medical Genetics, 2024, v. 17, n. 1, p. 65, doi. 10.29409/ijcmg.v17i1.356

By:

Ali, Amal Mohammed;
Almukhtar, Asmaa Amer;
Ismail, Noor Hashim;
Majeed, Ayeda M.;
Thaer, Noor;
Mutlak, Fatima Abd;
Alrahman, Shaimaa Abdul

Publication type:

Article

染色体核型异常、Th17/Treg 免疫失衡与复发性流产的关系及其影响因素分析.

Published in:

Progress in Modern Biomedicine, 2023, v. 23, n. 11, p. 2149, doi. 10.13241/j.cnki.pmb.2023.11.029

By:

魏淑彦;
杨会欣;
潘雪娇;
文晓燕;
贾立云

Publication type:

Article

Screening for chromosome abnormalities by microscopic chromosome analysis: A report of 2 years study of cytogenetic results of referred candidate for prenatal diagnosis.

Published in:

Iranian Journal of Reproductive Medicine, 2013, p. 27

By:

Dehghani, M. R.;
Arrigo, G.;
Hashemian, Z.;
Zuffardi, O.

Publication type:

Article

Overview of Chromosome Abnormalities in First Trimester Miscarriages: A Series of 1,011 Consecutive Chorionic Villi Sample Karyotypes.

Published in:

Cytogenetic & Genome Research, 2017, v. 152, n. 2, p. 81, doi. 10.1159/000477707

By:

Soler, anna;
Morales, Carme;
Mademont-Soler, Irene;
Margarit, Ester;
Borrell, antoni;
Borobio, Virginia;
Muñoz, Miriam;
Sánchez, aurora

Publication type:

Article

Chromosome Abnormality Detection Using Flying Fox Optimization based Deep Convolutional Neural Network.

Published in:

International Journal of Intelligent Engineering & Systems, 2025, v. 18, n. 4, p. 496, doi. 10.22266/ijies2025.0531.32

By:

Devika, Potta;
Begum, Samreen;
Dasari, Renuka;
Javangula, Vamsi Nath;
Shaik, Abdul Hameed

Publication type:

Article

Variables Influencing Pregnancy Termination Following Prenatal Diagnosis of Fetal Chromosome Abnormalities.

Published in:

Journal of Genetic Counseling, 2013, v. 22, n. 2, p. 238, doi. 10.1007/s10897-012-9539-1

By:

Hawkins, Anne;
Stenzel, Ana;
Taylor, Joanne;
Chock, Valerie;
Hudgins, Louanne

Publication type:

Article

A special type of chromosome 1 abnormality in myelodysplastic syndrome patients: duplication 1q.

Published in:

British Journal of Haematology, 2020, v. 189, n. 5, p. e218, doi. 10.1111/bjh.16643

By:

Yu, Yan;
Zhang, Tongtong;
Zeng, Zhao;
Wang, Qinrong;
Hong, Yang;
Shen, Hongjie;
Wu, Depei;
Pan, Jinlan;
Chen, Suning;
Sun, Aining

Publication type:

Article

Azacitidine improves outcome in higher‐risk MDS patients with chromosome 7 abnormalities: a retrospective comparison of GESMD and GFM registries.

Published in:

British Journal of Haematology, 2018, v. 181, n. 3, p. 350, doi. 10.1111/bjh.15190

By:

Díez‐Campelo, María;
Lorenzo, Jose I.;
Itzykson, Raphael;
Rojas, Silvia M.;
Berthon, Céline;
Luño, Elisa;
Beyne‐Rauzy, Odile;
Perez‐Oteyza, Jaime;
Vey, Norbert;
Bargay, Joan;
Park, Sophie;
Cedena, Teresa;
Bordessoule, Dominique;
Muñoz, Juan A.;
Gyan, Emmanuel;
Such, Esperanza;
Visanica, Sorin;
López‐Cadenas, Félix;
de Botton, Stéphane;
Hernández‐Rivas, Jesús M.

Publication type:

Article

Cell-Free DNA Screening for Sex Chromosome Abnormalities and Pregnancy Outcomes, 2018–2020: A Retrospective Analysis.

Published in:

Journal of Personalized Medicine, 2022, v. 12, n. 1, p. 48, doi. 10.3390/jpm12010048

By:

Lu, Yanmei;
Zhou, Shihao;
Linpeng, Siyuan;
Ding, Siyi;
Li, Shihong;
Li, Yujiao;
Shi, Liangcheng;
He, Jun;
Liu, Yalan

Publication type:

Article

FISH studies of chromosome abnormalities in germ cells and its relevance in reproductive counseling.

Published in:

Asian Journal of Andrology, 2005, v. 7, n. 3, p. 227, doi. 10.1111/j.1745-7262.2005.00061.x

By:

Sarrate, Zaida;
Blanco, Joan;
Anton, Ester;
Egozcue, Susana;
Egozcue, Josep;
Vidal, Francesca

Publication type:

Article

Myelodysplastic syndrome with chromosome 5 abnormalities: a nationwide survey in Japan.

Published in:

Leukemia (08876924), 2008, v. 22, n. 10, p. 1874, doi. 10.1038/leu.2008.199

By:

Tasaka, T.;
Tohyama, K.;
Kishimoto, M.;
Ohyashiki, K.;
Mitani, K.;
Hotta, T.;
Kanamaru, A.;
Okamoto, S.;
Karasawa, M.;
Kimura, A.;
Tomonaga, M.;
Uchiyama, T.;
Ozawa, K.

Publication type:

Article

Non-invasive prenatal testing - a new method in improving first trimester screening for chromosome-related abnormalities.

Published in:

Gineco.eu, 2016, v. 12, n. 3, p. 146, doi. 10.18643/gieu.2016.146

By:

Vasilescu, Sorin;
Munteanu, Octavian;
Radu, Gabriel;
Voicu, Diana;
Dumitrascu, Mihai;
Vartej, Petrache;
Bohiltea, Roxana;
Vladareanu, Simona;
Cirstoiu, Monica

Publication type:

Article

Chromosome 16 Abnormalities in Embryos and in Sperm from a Male with a Fragile Site at 16q22.1.

Published in:

Cytogenetic & Genome Research, 2014, v. 142, n. 2, p. 134, doi. 10.1159/000357411

By:

Martorell, M.R.;
Martínez-Pasarell, O.;
Lopez, O.;
Polo, a.;
Sandalinas, M.;
Garcia-Guixé, E.;
Bassas, L.

Publication type:

Article

Polymorphisms Within DNA Double-Strand Breaks Repair-Related Genes Contribute to Structural Chromosome Abnormality in Recurrent Pregnancy Loss.

Published in:

Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.787718

By:

Cheng, Zhenbo;
Cheng, Dehua;
Li, Jiancheng;
Guo, Lihuang;
Zhang, Wei;
Zhang, Conghui;
Liu, Yangxu;
Huang, Yue;
Xu, Keqian

Publication type:

Article

Pedigree analysis of two brothers with severe oligozoospermia caused by maternal inv(X) (p22.3, q22) chromosome abnormality.

Published in:

Andrologia, 2020, v. 52, n. 6, p. 1, doi. 10.1111/and.13602

By:

Ge, Yunsheng;
Sha, Yanwei;
Cai, Meijiao;
Chen, Xiaolu;
Sha, Yankun;
Xu, Xiaohui

Publication type:

Article

Diagnostic cytogenetic testing following positive noninvasive prenatal screening results of sex chromosome abnormalities: Report of five cases and systematic review of evidence.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 7, p. 1, doi. 10.1002/mgg3.1297

By:

Xie, Xiaolei;
Tan, Weihe;
Li, Fuguang;
Carrano, Eric;
Ramirez, Paola;
DiAdamo, Autumn;
Grommisch, Brittany;
Amato, Katherine;
Chai, Hongyan;
Wen, Jiadi;
Li, Peining

Publication type:

Article

Myelodysplastic syndrome in transformation to acute myeloid leukemia presenting with diabetes insipidus: due to pituitary infiltration association with abnormalities of chromosomes 3 and 7.

Published in:

European Journal of Haematology, 2002, v. 69, n. 2, p. 115, doi. 10.1034/j.1600-0609.2002.02763.x

By:

Müller, Claudia I.;
Engelhardt, Monika;
Laubenberger, Jörg;
Kunzmann, Regina;
Engelhardt, Rupert;
Lübbert, Michael

Publication type:

Article

Additional Chromosome Abnormalities, BCR-ABL Tyrosine Kinase Domain Mutations and Clinical Outcome in Hungarian Tyrosine Kinase Inhibitor-Resistant Chronic Myelogenous Leukemia Patients.

Published in:

Acta Haematologica, 2011, v. 127, n. 1, p. 34, doi. 10.1159/000331472

By:

Meggyesi, Nóra;
Kozma, András;
Halm, Gabriella;
Nahajevszky, Sarolta;
Bátai, Árpád;
Fekete, Sándor;
Barta, Anikó;
Ujj, György;
Lueff, Sándor;
Sipos, Andrea;
Ádám, Emma;
Bors, András;
Reményi, Péter;
Masszi, Tamás;
Tordai, Attila;
Andrikovics, Hajnalka

Publication type:

Article

Analysis of chromosome abnormalities in the Asian swamp eel (Monopterus albus) affected by arsenic contamination near a gold mine area.

Published in:

International Journal of Environmental Studies, 2020, v. 77, n. 5, p. 815, doi. 10.1080/00207233.2019.1704087

By:

Neeratanaphan, Lamyai;
Kanjanakunti, Arunya;
Intamat, Somsak;
Tengjaroenkul, Bundit

Publication type:

Article

T-cell lineage acute lymphoblastic leukemia with chromosome 5 abnormality in a patient with Crohn's disease and lipoid nephrosis.

Published in:

2000

By:

Pá;rard, L.;
Thomas, X.;
Jaumain, H.;
Theuil, G.;
Bret, M.;
Coronel, B.;
Charrin, C.;
Boulétreau, P.;
Pérard, L;
Boulétreau, P

Publication type:

journal article

Detection of Chromosome Abnormalities by Quantitative Fluorescent PCR in Ectopic Pregnancies.

Published in:

Gynecologic & Obstetric Investigation, 2005, v. 60, n. 3, p. 139, doi. 10.1159/000086131

By:

Goddijn, Mariette;
Van Stralen, Marja;
Schuring-Blom, Heleen;
Redeker, Bert;
Van Leeuwen, Liesbeth;
Repping, Sjoerd;
Leschot, Nico;
Van der Veen, Fulco

Publication type:

Article

The clinical performance of fetal sex chromosome abnormalities in serum biochemical screening in the second trimester.

Published in:

Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-78724-5

By:

Luo, Wei;
He, Bin;
Han, Daiwen;
Yuan, Lixing;
Tang, Jun;
Pang, Ling;
Zhao, Kai;
Zou, Fene;
Zhu, Qian;
Liu, Shanling

Publication type:

Article

新发 9 号染色体异常患儿的临床和细胞遗传学研究.

Published in:

Chinese Journal of Contemporary Pediatrics, 2018, v. 20, n. 1, p. 52, doi. 10.7499/j.issn.1008-8830.2018.01.011

By:

陆碧玉;
谭建强;
袁德健;
王文丹;
韦小妮;
严提珍;
蔡稔

Publication type:

Article

Current genetic counseling practice in the United States following positive non‐invasive prenatal testing for sex chromosome abnormalities.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 4, p. 802, doi. 10.1002/jgc4.1122

By:

Fleddermann, Lauren;
Hashmi, Syed Shahrukh;
Stevens, Blair;
Murphy, Lauren;
Rodriguez‐Buritica, David;
Friel, Lara A.;
Singletary, Claire

Publication type:

Article

Venous ulceration in males with sex chromosome abnormalities.

Published in:

Journal of the Royal Society of Medicine, 1993, v. 86, n. 1, p. 24

By:

Baker, S. R.;
Northeast, A. D. R.;
Berry, A. C.;
Burnand, K. G.

Publication type:

Article

Chromosome Abnormalities and Viability of Vitrified Eight-Cell Mouse Embryos at Presence of Two Different Cryoprotectants at Different Storage Durations.

Published in:

Cell Journal (Yakhteh), 2012, v. 14, n. 4, p. 254

By:

Zarei Moradi, Shabnam;
Mohseni Meybodi, Anahita;
Gourabi, Hamid;
Mozdarani, Hossein;
Mansouri, Zahra

Publication type:

Article

Prenatal Diagnosis of Chromosome Abnormalities: A 13-Year Institution Experience.

Published in:

Diagnostics (2075-4418), 2012, v. 2, n. 4, p. 57, doi. 10.3390/diagnostics2040057

By:

Comas, Carmen;
Echevarria, Mónica;
Rodríguez, María Ángeles;
Rodríguez, Ignacio;
Serra, Bernat;
Cirigliano, Vincenzo

Publication type:

Article

Differential prognostic impact of stratified additional chromosome abnormalities on disease progression among Malaysian chronic myeloid leukemia patients undergoing treatment with imatinib mesylate.

Published in:

Frontiers in Oncology, 2022, v. 12, p. 1, doi. 10.3389/fonc.2022.720845

By:

Mariam, Ismail Siti;
Norhidayah, Ramli;
Zulaikha, Abu Bakar;
Nazihah, Mohd Yunus;
Rosline, Hassan;
Kausar, Ghazali Anis;
Sarina, Sulong;
Azlan, Husin;
Ankathil, Ravindran

Publication type:

Article

Pathogenesis, clinical characteristics and personalized managements of multiple myeloma with chromosome 1 abnormalities.

Published in:

Leukemia & Lymphoma, 2023, v. 64, n. 8, p. 1373, doi. 10.1080/10428194.2023.2216325

By:

Zhou, Pan;
Li, Weiya;
Zuo, Suqiong;
Ma, Rongjun;
Yuan, Xiaoli;
Zhu, Zunmin

Publication type:

Article

TÜR OLUŞUMUNA NEDEN OLAN BAZI KROMOZOM ANORMALLİKLERİ.

Published in:

Anadolu University Journal of Sciences & Technology, 2007, v. 8, n. 2, p. 291

By:

Kaymak, Fisun

Publication type:

Article

Efficacy of maternal serum screening in the prenatal detection of fetal chromosome abnormalities in Japanese women.

Published in:

2000

By:

Kishida, Tatsuro;
Hoshi, Nobuhiko;
Hattori, Rifumi;
Negishi, Hiroaki;
Yamada, Hideto;
Okuyama, Kazuhiko;
Hanatani, Kaoru;
Takagi, Tsukasa;
Sagawa, Tadashi;
Fujimoto, Seiichiro;
Kishida, T;
Hoshi, N;
Hattori, R;
Negishi, H;
Yamada, H;
Okuyama, K;
Hanatani, K;
Takagi, T;
Sagawa, T;
Fujimoto, S

Publication type:

journal article

Chromosome abnormalities in 118 couples with recurrent spontaneous abortions.

Published in:

1984

By:

Tóth, A.;
Gaál, M.;
Bösze, P.;
László, J.;
Tóth, A;
Gaál, M;
Bösze, P;
László, J

Publication type:

journal article

Clinical experience of noninvasive prenatal testing for rare chromosome abnormalities in singleton pregnancies.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.955694

By:

Ting Hu;
Jiamin Wang;
Qian Zhu;
Zhu Zhang;
Rui Hu;
Like Xiao;
Yunyuan Yang;
Na Liao;
Sha Liu;
He Wang;
Xiaoyu Niu;
Shanling Liu

Publication type:

Article

The Possible Role of Chronic Infection in the Etiopathogenesis of a Case of 5q-Syndrome Associated with Tuberculosis and Abnormality of the X Chromosome.

Published in:

Mediterranean Journal of Hematology & Infectious Diseases, 2022, v. 14, n. 1, p. 1, doi. 10.4084/MJHID.2022.079

By:

Mitev, Lubomir;
Grahlyova, Liliya;
Kancheva, Tatiana

Publication type:

Article

Lipoatrophic panniculitis and chromosome 10 abnormality.

Published in:

European Journal of Pediatric Dermatology, 2012, v. 22, n. 3, p. 182

By:

Moramarco, F.;
Garofalo, L.;
Milano, A.;
Bonifazi, E.

Publication type:

Article

Preimplantation genetic testing is not a preferred recommendation for patients with X chromosome abnormalities.

Published in:

2021

By:

Li, Chenxi;
Dang, Yujie;
Li, Jing;
Li, Hongchang;
Zhu, Yueting;
Qin, Yingying

Publication type:

journal article

The Types and Frequencies of X Chromosome Abnormalities in Women with Reproductive Problems.

Published in:

Cytogenetic & Genome Research, 2024, v. 163, n. 5/6, p. 274, doi. 10.1159/000534428

By:

Kouvidi, Elisavet;
Tsarouha, Haralambia;
Zachaki, Sophia;
Katsidi, Christina;
Tsimela, Hara;
Pantou, Amelia;
Kanavakis, Emmanuel;
Mavrou, Ariadni

Publication type:

Article

Genetic screening for chromosomal abnormalities and Y chromosome microdeletions in Chinese infertile men.

Published in:

Journal of Assisted Reproduction & Genetics, 2012, v. 29, n. 6, p. 521, doi. 10.1007/s10815-012-9741-y

By:

Fu, Li;
Xiong, Da-Ke;
Ding, Xian-Ping;
Li, Chuang;
Zhang, Li-Yuan;
Ding, Min;
Nie, Shuang-Shuang;
Quan, Qiang

Publication type:

Article

Cytogenetic Studies of Chromosome Abnormalities in Thyroid Cancer Patients Before and After Iodine-131 Treatment.

Published in:

Bezmialem Science, 2019, v. 7, n. 2, p. 118, doi. 10.14235/bas.galenos.2018.2571

By:

ÖDEN, Seda;
ATASOY, Sezen;
DEMİR, Mustafa;
DEVİREN, Ayhan

Publication type:

Article

Abnormalities in chromosome 6q24 as a cause of early-onset, non-obese, non-autoimmune diabetes mellitus without history of neonatal diabetes.

Published in:

Diabetic Medicine, 2015, v. 32, n. 7, p. 963, doi. 10.1111/dme.12758

By:

Yorifuji, T.;
Matsubara, K.;
Sakakibara, A.;
Hashimoto, Y.;
Kawakita, R.;
Hosokawa, Y.;
Fujimaru, R.;
Murakami, A.;
Tamagawa, N.;
Hatake, K.;
Nagasaka, H.;
Suzuki, J.;
Urakami, T.;
Izawa, M.;
Kagami, M.

Publication type:

Article