Cytogenetic analysis and family research for two cases of chromosome 6 microduplication and chromosome 9 microdeletion: Different clinical manifestations

[1]  Xing Wu,et al.  Prenatal features of 17q12 microdeletion and microduplication syndromes: A retrospective case series. , 2021, Taiwanese journal of obstetrics & gynecology.

[2]  Yufan Li,et al.  A cross-sectional survey of pregnant women's knowledge of chromosomal aneuploidy and microdeletion and microduplication syndromes. , 2020, European journal of obstetrics, gynecology, and reproductive biology.

[3]  Shaobin Lin,et al.  Absence of heterozygosity detected by single‐nucleotide polymorphism array in prenatal diagnosis , 2019, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

[4]  P. Bokariya,et al.  A Study on Chromosomal Analysis of Patients with Primary Amenorrhea , 2019, Journal of human reproductive sciences.

[5]  F. Vialard,et al.  First prenatal diagnosis of a ‘pure’ 9q34.3 deletion (Kleefstra syndrome): A case report and literature review , 2018, The journal of obstetrics and gynaecology research.

[6]  B. Levy,et al.  Prenatal diagnosis by chromosomal microarray analysis. , 2018, Fertility and sterility.

[7]  Ivanov Hy,et al.  Rare Case of a Heterozygous Microdeletion 9q21.11-q21.2: Clinical and Genetic Characteristics. , 2018, Balkan journal of medical genetics : BJMG.

[8]  S. Kapoor,et al.  Cytogenetic Analysis for Suspected Chromosomal Abnormalities; A Five Years Experience. , 2016, Journal of clinical and diagnostic research : JCDR.

[9]  B. Bernhardt,et al.  An Exploration of Genetic Counselors’ Needs and Experiences with Prenatal Chromosomal Microarray Testing , 2014, Journal of Genetic Counseling.

[10]  Y. Shen,et al.  Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray‐based analysis , 2013, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

[11]  I. Simonic,et al.  A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial features. , 2013, European journal of medical genetics.

[12]  Jiyun Lee,et al.  Delineation of Subtelomeric Deletion of the Long Arm of Chromosome 6 , 2011, Annals of human genetics.

[13]  A. Villa,et al.  Interstitial tandem duplication of 6p: a case with partial trisomy (6)(p12p21.3). , 2000, American journal of medical genetics.

[14]  J. Berns,et al.  Duplication 6q syndrome. , 1979, American journal of medical genetics.