Literature DB >> 9826907

Cri-du-chat syndrome diagnosed by amniocentesis performed due to abnormal maternal serum test.

L Fankhauser, A M Brundler, S Dahoun.   

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Year:  1998        PMID: 9826907

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


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  5 in total

Review 1.  5p deletions: Current knowledge and future directions.

Authors:  Joanne M Nguyen; Krista J Qualmann; Rebecca Okashah; AmySue Reilly; Mikhail F Alexeyev; Dennis J Campbell
Journal:  Am J Med Genet C Semin Med Genet       Date:  2015-08-03       Impact factor: 3.908

Review 2.  Cri du Chat syndrome.

Authors:  Paola Cerruti Mainardi
Journal:  Orphanet J Rare Dis       Date:  2006-09-05       Impact factor: 4.123

3.  Partial trisomy 4q and monosomy 5p inherited from a maternal translocationt(4;5)(q33; p15) in three adverse pregnancies.

Authors:  Jingbo Zhang; Bei Zhang; Tong Liu; Huihui Xie; Jingfang Zhai
Journal:  Mol Cytogenet       Date:  2020-06-30       Impact factor: 2.009

4.  Prenatal Sonographic Features of Cri-du-Chat Syndrome: A Case Report and Analytical Literature Review.

Authors:  Kuntharee Traisrisilp; Yuri Yanase; Srimeunwai Ake-Sittipaisarn; Theera Tongsong
Journal:  Diagnostics (Basel)       Date:  2022-02-06

5.  Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature.

Authors:  Jiasun Su; Huayu Fu; Bobo Xie; Weiliang Lu; Wei Li; Yuan Wei; Qiang Zhang; Shengkai Wei; Qiuli Chen; Yingchi Lu; Tingting Jiang; Jingsi Luo; Zailong Qin
Journal:  Mol Cytogenet       Date:  2019-12-09       Impact factor: 2.009

  5 in total

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