Molecular study of 45,X conceptuses: Correlation with clinical findings
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference17 articles.
1. Congenital cystic hygroma of the neck diagnosed prenatally: Outcome with normal and abnormal karyotype
2. A cytogenetic and molecular study of a series of 45,X fetuses and their parents.
3. Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22
4. Improved DNA markers for efficient analysis of fragile X families
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2. Hidden Y Chromosome Material and Congenital Cardiovascular Malformations in a Cohort of Turner Syndrome Patients with 45,X Blood Karyotype;Cytogenetic and Genome Research;2023-12-21
3. Prenatal diagnosis of sex chromosome aneuploidy—What do we tell the prospective parents?;Prenatal Diagnosis;2022-11-09
4. Effect of the parental origin of the X-chromosome on the clinical features, associated complications, the two-year-response to growth hormone (rhGH) and the biochemical profile in patients with turner syndrome;International Journal of Pediatric Endocrinology;2013-06-04
5. Parental origin of the X chromosome, X chromosome mosaicism and screening for “hidden” Y chromosome in 45,X Turner syndrome ascertained cytogenetically;Clinical Genetics;2008-06-28
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