Results 1 to 10 of about 4,037 (109)
Supernumerary Marker Chromosome Identified in Asian Elephant (Elephas maximus) [PDF]
Animals, 2023 We identified a small, supernumerary marker chromosome (sSMC) in two phenotypically normal Asian elephants (Elephas maximus): a female (2n = 57,XX,+mar) and her male offspring (2n = 57,XY,+mar). sSMCs are defined as structurally abnormal chromosomes that
Halina Cernohorska +5 more
doaj +2 more sources
Male Infertility Associated with a Supernumerary Marker Chromosome [PDF]
The World Journal of Men's Health, 2017 A marker chromosome (mar) is a structurally abnormal chromosome in which no part can be identified. The significance of a marker varies, depending on the material contained within the marker.
Seung-Hun Song +5 more
doaj +2 more sources
Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing [PDF]
Biomedicines, 2021 Interpreting the clinical significance of small supernumerary marker chromosomes (sSMCs) in prenatal diagnosis is still an urgent problem in genetic counselling regarding the fate of a pregnancy. We present a case of prenatal diagnosis of mosaic sSMC(10)
Igor N. Lebedev +13 more
doaj +2 more sources
Taiwanese Journal of Obstetrics & Gynecology, 2017 Objective: We present the association of paternal uniparental disomy (UPD) 9 with mosaicism for a small supernumerary marker chromosome 9 [sSMC(9)] and a supernumerary ring chromosome 9 [r(9)].
Chih-Ping Chen +10 more
doaj +3 more sources
Taiwanese Journal of Obstetrics & Gynecology, 2020 Objective: To present molecular cytogenetic characterization of mosaic supernumerary ring chromosome 8 which has trisomy of a region of chromosome 8p12-q21.13 associated with congenital hypoplasia of the tongue and review of the literature.
Hui-Yuan Shao +4 more
doaj +3 more sources
Small Supernumerary Marker Chromosome (sSMC) 15 in Male Primary Infertility: A Case Study [PDF]
Case Reports in MedicineThis case report describes a 39-year-old phenotypically normal male patient of a married couple with primary infertility presenting as candidates for assisted reproductive techniques.
Filomena Mottola +4 more
doaj +2 more sources
Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22- A Case Report [PDF]
Iranian Journal of Public Health, 2016 The interpretation of supernumerary chromosome is important for genetic counseling and prognosis. Here, we used SNP array and conventional karyotyping method to identify a denovo marker chromosome originated from chromosome 22 and 11 in a newborn ...
Mohammad Yahya VAHIDI MEHRJARDI +4 more
doaj +1 more source
Identification of a Small Supernumerary Marker Chromosome in a Turner Syndrome Patient with Karyotype mos 46,X,+mar/45,X [PDF]
Genes, 2023 exaly +2 more sources
Taiwanese Journal of Obstetrics & Gynecology, 2010 Objective: To present prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 8 by multiplex ligation-dependent probe amplification (MLPA), fluorescence in situ hybridization
Chih-Ping Chen +9 more
doaj +3 more sources
Taiwanese Journal of Obstetrics & Gynecology, 2017 Objective: We present prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 16. Case report: A 28-year-old woman underwent amniocentesis at 17 weeks of gestation because of
Chih-Ping Chen +8 more
doaj +3 more sources