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Correspondence on "The views of people with a lived experience of deafness and the general public regarding genetic testing for deafness in the reproductive setting: A systematic review" by Freeman et al.

  • Authors : Li J; Medical Genetics Center, Lanzhou Maternal and Child Health Hospital, Gansu, China.; Sun X

Subjects: Genetic Testing* ; Deafness*/Deafness*/Deafness*/diagnosis ; Deafness*/Deafness*/Deafness*/genetics

  • Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2023 Jan; Vol. 25 (1), pp. 155-156. Date of Electronic Publication: 2022 Nov 14.Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Live Birth with or without Preimplantation Genetic Testing for Aneuploidy.

  • Authors : Yan J; From the Center for Reproductive Medicine, Cheeloo College of Medicine, Key Laboratory of Reproductive Endocrinology of the Ministry of Education, and the National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Shandong University, Shandong Key Laboratory of Reproductive Medicine, and Shandong Provincial Clinical Research Center for Reproductive Health, Jinan (J.Y., Y.Q., H.Z., D.W., J.L., T.N., W.Z., K.W., Y.G., Y.S., Z.-J.C.), the Center for Reproductive Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai Key Laboratory for Assisted Reproduction and Reproductive Genetics (Y.S., Z.-J.C., Y.L., T.Z.), and the Obstetrics and Gynecology Hospital of Fudan University, Shanghai JIAI Genetics and IVF Institute, Key Laboratory of Female Reproductive Endocrine Related Diseases, Obstetrics and Gynecology Hospital of Fudan University (X.S., J.F.), Shanghai, the Institute of Reproductive and Stem Cell Engineering, School of Basic Medical Science, Central South University, and Reproductive and Genetic Hospital of CITIC-Xiangya, Changsha (F.G., H.M.), the Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, National Clinical Research Center for Obstetrics and Gynecology, Key Laboratory of Assisted Reproduction, Ministry of Education, and Beijing Key Laboratory of Reproductive Endocrinology and Assisted Reproductive Technology, Beijing (R.L.), the Department of Reproductive Medicine, the Affiliated Obstetrics and Gynecology Hospital with Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital (X.L., J.Z.), and the Department of Reproductive Medicine, First Affiliated Hospital of Nanjing Medical University-Jiangsu Province Hospital (X.M., W.W.), Nanjing, the Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Suzhou (H.L., Q.M.), the Center for Reproductive Medicine of Yantai Yuhuangding Hospital, Yantai (C.H.), the Center of Reproductive Medicine, Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Key Laboratory of Reproductive Dysfunction Diseases and Fertility Remodeling of Liaoning Province, Shenyang (J.T.), the Center for Reproductive Medicine, Wuhan University, Wuhan (J.Y.), the Department of Reproductive Endocrinology, Key Laboratory of Reproductive Genetics, Ministry of Education, Women's Reproductive Health Laboratory of Zhejiang Province, Women's Hospital, Zhejiang University School of Medicine, Hangzhou (Y.Z.), the Department of Reproductive Health and Infertility, Guangdong Women and Children Hospital, Guangzhou (F.L.), and the Reproductive Medicine Center, Department of Obstetrics and Gynecology, the First Affiliated Hospital of Anhui Medical University, Hefei (D.C.) - all in China; the Department of Biostatistics, Yale University School of Public Health, New Haven, CT (H.Z.)

Subjects: Aneuploidy* ; Fertilization in Vitro* ; Genetic Testing*

  • Source: The New England journal of medicine [N Engl J Med] 2021 Nov 25; Vol. 385 (22), pp. 2047-2058.Publisher: Massachusetts Medical Society Country of Publication: United States NLM ID: 0255562 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

A comprehensive and universal approach for embryo testing in patients with different genetic disorders.

  • Authors : Zhang S; Shanghai Ji Ai Genetics & IVF Institute, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.; Lei C

Subjects: Genetic Diseases, Inborn/Genetic Diseases, Inborn/Genetic Diseases, Inborn/*diagnosis ; Genetic Testing/Genetic Testing/Genetic Testing/*methods; Aneuploidy

  • Source: Clinical and translational medicine [Clin Transl Med] 2021 Jul; Vol. 11 (7), pp. e490.Publisher: Wiley Country of Publication: United States NLM ID: 101597971 Publication Model: Print Cited Medium: Internet ISSN: 2001-1326

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Academic Journal

Genetic etiologic analysis in 74 Chinese Han women with idiopathic premature ovarian insufficiency by combined molecular genetic testing.

  • Authors : Shen J; State Key Laboratory of Reproductive Medicine, Center of Clinical Reproductive Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, China.; Qu D

Subjects: Genetic Testing*; Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/*genetics ; Primary Ovarian Insufficiency/Primary Ovarian Insufficiency/Primary Ovarian Insufficiency/*genetics

  • Source: Journal of assisted reproduction and genetics [J Assist Reprod Genet] 2021 Apr; Vol. 38 (4), pp. 965-978. Date of Electronic Publication: 2021 Feb 04.Publisher: Springer Country of Publication: Netherlands NLM ID: 9206495 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

BasePhasing: a highly efficient approach for preimplantation genetic haplotyping in clinical application of balanced translocation carriers.

  • Authors : Zhang S; Shanghai Ji Ai Genetics & IVF Institute, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, 200011, China.; State Key Laboratory of Genetic Engineering, Collaborative Innovation Center for Genetics and Development, School of Life Science, Fudan University, 588 Fangxie Rd, Shanghai, 200438, China.

Subjects: Haplotypes*; Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Preimplantation Diagnosis/Preimplantation Diagnosis/Preimplantation Diagnosis/*methods

  • Source: BMC medical genomics [BMC Med Genomics] 2019 Mar 18; Vol. 12 (1), pp. 52. Date of Electronic Publication: 2019 Mar 18.Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794

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Academic Journal

Identification of gross deletions in FBN1 gene by MLPA.

  • Authors : Yang H; State Key Laboratory of Cardiovascular Disease, Beijing Key Laboratory for Molecular Diagnostics of Cardiovascular Diseases, Diagnostic Laboratory Service, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.; Ma Y

Subjects: Genetic Testing*; Fibrillin-1/Fibrillin-1/Fibrillin-1/*genetics ; Marfan Syndrome/Marfan Syndrome/Marfan Syndrome/*genetics

  • Source: Human genomics [Hum Genomics] 2018 Oct 04; Vol. 12 (1), pp. 46. Date of Electronic Publication: 2018 Oct 04.Publisher: BioMed Central Country of Publication: England NLM ID: 101202210 Publication Model: Electronic Cited Medium: Internet ISSN: 1479-7364

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Academic Journal

Non-invasive pre-implantation aneuploidy screening and diagnosis of beta thalassemia IVSII654 mutation using spent embryo culture medium.

  • Authors : Liu W; a Department of Clinical Laboratory of Gynecology and Obstetrics, Key Laboratory for Reproduction and Genetics of Guangdong Higher Education Institutes, Key Laboratory for Major Obstetric Diseases of Guangdong Province , Third Affiliated Hospital of Guangzhou Medical University , Guangzhou , PR China.; Liu J

Subjects: Culture Media/Culture Media/Culture Media/*analysis ; Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Hemoglobins/Hemoglobins/Hemoglobins/*genetics

  • Source: Annals of medicine [Ann Med] 2017 Jun; Vol. 49 (4), pp. 319-328. Date of Electronic Publication: 2016 Dec 14.Publisher: Informa Healthcare Country of Publication: England NLM ID: 8906388 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Genetic testing of the FBN1 gene in Chinese patients with Marfan/Marfan-like syndrome.

  • Authors : Yang H; State Key Laboratory of Cardiovascular Disease, Beijing Key Laboratory for Molecular Diagnostics of Cardiovascular Diseases, Diagnostic Laboratory Service, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100037, People's Republic of China.; Luo M

Subjects: Genetic Testing* ; Mutation*; Fibrillin-1/Fibrillin-1/Fibrillin-1/*genetics

  • Source: Clinica chimica acta; international journal of clinical chemistry [Clin Chim Acta] 2016 Aug 01; Vol. 459, pp. 30-35. Date of Electronic Publication: 2016 May 24.Publisher: Elsevier Country of Publication: Netherlands NLM ID: 1302422 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Telomerase reverse transcriptase gene promoter mutations help discern the origin of urogenital tumors: a genomic and molecular study.

  • Authors : Wu S; Shenzhen Second People's Hospital, the First Affiliated Hospital of Shenzhen University, Shenzhen, China; Department of Urology, Sun Yat-Sen University Cancer Center, Guangzhou, China

Subjects: DNA Mutational Analysis* ; Mutation* ; Promoter Regions, Genetic*

  • Source: European urology [Eur Urol] 2014 Feb; Vol. 65 (2), pp. 274-7. Date of Electronic Publication: 2013 Nov 05.Publisher: Elsevier Science Country of Publication: Switzerland NLM ID: 7512719 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Prediction of autism susceptibility genes based on association rules.

  • Authors : Gong L; State Key Laboratory of Bioelectronics, Department of Biological Science and Medical Engineering, Southeast University, Nanjing, People's Republic of China.; Yan Y

Subjects: Autistic Disorder/Autistic Disorder/Autistic Disorder/*genetics ; Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*methods

  • Source: Journal of neuroscience research [J Neurosci Res] 2012 Jun; Vol. 90 (6), pp. 1119-25. Date of Electronic Publication: 2012 Feb 16.Publisher: Wiley Interscience Country of Publication: United States NLM ID: 7600111 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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