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Results 1 to 25 of 258

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Molecular Mechanisms in 22q11 Deletion SyndromeWILLIAMS, Nigel M.Schizophrenia bulletin. 2011, Vol 37, Num 5, pp 882-889, issn 0586-7614, 8 p.Article

Reduced expression of Mad2 and Bub I proteins is associated with spontaneous miscarriagesQIONG SHI; MIN HU; MIN LUO et al.Molecular human reproduction. 2011, Vol 17, Num 1-2, pp 14-21, issn 1360-9947, 8 p.Article

Evaluation of genome coverage and fidelity of multiple displacement amplification from single cells by SNP arrayJIAWEI LING; GUANGLUN ZHUANG; TAZON-VEGA, Barbara et al.Molecular human reproduction. 2009, Vol 15, Num 11-12, pp 739-747, issn 1360-9947, 9 p.Article

Clinical relevance of diagnosing structural chromosome abnormalities in couples with repeated miscarriageGODDIJN, M; JOOSTEN, J. H. K; KNEGT, A. C et al.Human reproduction (Oxford. Print). 2004, Vol 19, Num 4, pp 1013-1017, issn 0268-1161, 5 p.Article

Autism geneticsPERSICO, Antonio M; NAPOLIONI, Valerio.Behavioural brain research. 2013, Vol 251, pp 95-112, issn 0166-4328, 18 p.Article

Amniocentesis Performed for Karyotyping after Identified Ultrasonographic Abnormalities: What to Expect?GAUDRY, Patrice; ESVAN, Maxime; MEYNARD, Jean-Baptiste et al.Fetal diagnosis and therapy. 2012, Vol 31, Num 1, pp 55-62, issn 1015-3837, 8 p.Article

A novel integrated microfluidic platform to perform fluorescence in situ hybridization for chromosomal analysisTAI, Chien-Hsuan; HO, Chung-Liang; CHEN, Ya-Lan et al.Microfluidics and nanofluidics (Print). 2013, Vol 15, Num 6, pp 745-752, issn 1613-4982, 8 p.Article

Elevated incidence of chromosomally chaotic embryos among frozen-thawed preimplantation embryosSALUMETS, Andres; HORELLI-KUITUNEN, Nina; SUIKKARI, Anne-Maria et al.European journal of obstetrics, gynecology, and reproductive biology. 2004, Vol 114, Num 1, pp 59-63, issn 0301-2115, 5 p.Article

Preimplantation genetic diagnosis by fluorescence in situ hybridization: Clinical possibilities and pitfallsPEHLIVAN, Tugce; RUBIO, Carmen; RODRIGO, Lorena et al.Journal of the Society for Gynecologic Investigation. 2003, Vol 10, Num 6, pp 315-322, issn 1071-5576, 8 p.Article

Identification of Chromosome Abnormalities in Subtelomeric Regions by Microarray Analysis : A Study of 5,380 CasesSHAO, Lina; SHAW, Chad A; PURSLEY, Amber N et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 17, pp 2242-2251, issn 1552-4825, 10 p.Article

Chromosomal Anomalies in the Etiology of Anorectal Malformations: A ReviewMARCELIS, Carlo; DE BLAAUW, Ivo; BRUNNER, Han et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 11, pp 2692-2704, issn 1552-4825, 13 p.Article

Chromosomal abnormality rate in human pre-embryos derived from in vitro fertilization cycles cultured in the presence of follicular-fluid meiosis activating sterol (FF-MAS)BERGH, Christina; LOFT, Anne; LUNDIN, Kersti et al.Human reproduction (Oxford. Print). 2004, Vol 19, Num 9, pp 2109-2117, issn 0268-1161, 9 p.Article

Baseline and treatment-induced chromosomal abnormalities in peripheral blood lymphocytes of Hodgkin's lymphoma patientsM'KACHER, R; GIRINSKY, T; CARDE, P et al.International journal of radiation oncology, biology, physics. 2003, Vol 57, Num 2, pp 321-326, issn 0360-3016, 6 p.Article

Chromosomal Abnormalities in Couples with Reproductive DisordersMEZA-ESPINOZA, Juan Pablo; ORTIZ ANGUIANO, Lilia; RIVERA, Horacio et al.Gynecologic and obstetric investigation. 2008, Vol 66, Num 4, pp 237-240, issn 0378-7346, 4 p.Article

Anesthesia for children with Wolf-Hirshhorn syndrome: a report and literature reviewMOHIUDDIN, Shireen; MAYHEW, James F.Paediatric anaesthesia (Paris). 2005, Vol 15, Num 3, pp 254-255, issn 1155-5645, 2 p.Article

DNA double strand breaks (DSB) and non-homologous end joining (NHEJ) pathways in human leukemiaRASSOOL, Feyruz Virgilia.Cancer letters. 2003, Vol 193, Num 1, pp 1-9, issn 0304-3835, 9 p.Article

Evaluation of cytological effects of Zn2+ in relation to germination and root growth of Nigella sativa L. and Triticum aestivum LEL-GHAMERY, A. A; EL-KHOLY, M. A; EL-YOUSSER, M. A et al.Mutation research. Genetic toxicology and environmental mutagenesis. 2003, Vol 537, Num 1, pp 29-41, issn 1383-5718, 13 p.Article

Chromosomal Abnormality in Patients with Secondary AmenorrheaSAFAI, Akbar; VASEI, Mohammad; ATTARANZADEH, Armin et al.Archives of Iranian medicine. 2012, Vol 15, Num 4, pp 232-234, 3 p.Article

Genetic aspects of human male infertility: the frequency of chromosomal abnormalities and Y chromosome microdeletions in severe male factor infertilityVICDAN, Arzu; VICDAN, Kubilay; GÜNALP, Serdar et al.European journal of obstetrics, gynecology, and reproductive biology. 2004, Vol 117, Num 1, pp 49-54, issn 0301-2115, 6 p.Article

Paternal reciprocal translocation t(11;16)(p13;q24.3) in a Silver-Russel syndrome patientVUNDINTI BABU RAO; LILY, Kerketta; SEEMA, Korgaonkar et al.Annales de génétique (Paris). 2003, Vol 46, Num 4, pp 475-478, issn 0003-3995, 4 p.Article

Cytogenetics and clinical features of pediatric myelodysplastic syndrome in JapanMORIWAKI, Koichi; MANABE, Atsushi; TAKETANI, Takeshi et al.International journal of hematology. 2014, Vol 100, Num 5, pp 478-484, issn 0925-5710, 7 p.Article

Phylloid Hypermelanosis and Melanocytic Nevi with Aggregated and Disfigured Melanosomes: Causal Relationship between Phylloid Pigment Distribution and Chromosome 13 AbnormalitiesOISO, Naoki; TSURUTA, Daisuke; IMANISHI, Hisayoshi et al.Dermatology (Basel). 2010, Vol 220, Num 2, pp 169-172, issn 1018-8665, 4 p.Article

Trends in Cytogenetic Testing and Identification of Chromosomal Abnormalities among Pregnancies and Children with Birth Defects, Metropolitan Atlanta, 1968-2005JACKSON, Jodi M; CRIDER, Krista S; RASMUSSEN, Sonja A et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 1, pp 116-123, issn 1552-4825, 8 p.Article

An association between sex chromosomal aneuploidy in sperm and an abortus with 45,X of paternal origin: possible transmission of chromosomal abnormalities through ICSITANG, S. S; GAO, H; ROBINSON, W. P et al.Human reproduction (Oxford. Print). 2004, Vol 19, Num 1, pp 147-151, issn 0268-1161, 5 p.Article

Analysis of chromosomal abnormalities in testicular and epididymal spermatozoa from azoospermic ICSI patients by fluorescence in-situ hybridizationRODRIGO, L; RUBIO, C; MATEU, E et al.Human reproduction (Oxford. Print). 2004, Vol 19, Num 1, pp 118-123, issn 0268-1161, 6 p.Article

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