Literature DB >> 2143821

Sex chromosome mosaicism not detected at amniocentesis.

B Roland1, D M Cox, N L Rudd.   

Abstract

Amniocentesis was performed because of a fetal abdominal wall defect, and a 45,X karyotype was obtained. A near-normal male infant with no features of Turner syndrome was delivered. The karyotype of the infant was 45,X/46,X,dic(Y)(q11), with each of the cell lines present in approximately 50 per cent of the lymphocytes and fibroblasts examined.

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Year:  1990        PMID: 2143821     DOI: 10.1002/pd.1970100509

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


  3 in total

1.  Prenatal and postnatal prevalence of Turner's syndrome: a registry study.

Authors:  C H Gravholt; S Juul; R W Naeraa; J Hansen
Journal:  BMJ       Date:  1996-01-06

2.  Clinical and molecular cytogenetic findings and pregnancy outcomes of fetuses with isochromosome Y.

Authors:  Yiqun He; Li Guo; Laiping Zheng; Congmian Ren; Ting Wang; Jian Lu
Journal:  Mol Cytogenet       Date:  2022-08-04       Impact factor: 1.904

3.  Clinical, cytogenetic, and molecular findings of isodicentric Y chromosomes.

Authors:  Yang Yang; Wang Hao
Journal:  Mol Cytogenet       Date:  2019-12-27       Impact factor: 2.009

  3 in total

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