Small supernumerary marker chromosome (sSMC) derived from chromosome 22 in an infertile man with hypogonadotropic hypogonadism
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s13353-011-0041-5.pdf
Reference19 articles.
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2. Colella S, Yau C, Taylor JM, Mirza G, Butler H, Clouston P et al (2007) QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data. Nucleic Acids Res 35:2013–2025
3. Crolla JA, Youings SA, Ennis S, Jacobs PA (2005) Supernumerary marker chromosomes in man: parental origin, mosaicism and maternal age revisited. Eur J Hum Genet 13(2):154–160
4. Kim HG, Bhagavath B, Layman LC (2008) Clinical manifestations of impaired GnRH neuron development and function. Neurosignals 16(2–3):165–182
5. Liehr T (2006) Familial small supernumerary marker chromosomes are predominantly inherited via the maternal line. Genet Med 8(7):459–462
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1. Hypogonadotropic hypogonadism associated with another small supernumerary marker chromosome (sSMC) derived from chromosome 22, a case report;Translational Andrology and Urology;2021-04
2. Molecular characterization of small supernumerary marker chromosomes derived from chromosome 14/22 detected in adult women with fertility problems;Medicine;2020-10-02
3. NR0B1 (DAX1) mutations in patients affected by congenital adrenal hypoplasia with growth hormone deficiency as a new finding;Journal of Applied Genetics;2013-02-02
4. Balanced reciprocal translocation t(5;13)(q33;q12) and 9q31.1 microduplication in a man suffering from infertility and pollinosis;Journal of Applied Genetics;2011-11-29
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