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Mindfulness-Based Psychoeducation App to Improve the Well-Being of Parents and Caregivers of Children With Autism: Development and Usability Study. [PDF]
Ma KKY +14 more
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Objective: We characterized a maternally inherited small supernumerary marker chromosome (sSMC) derived from chromosome 15 according to prenatal detection and made a review on the prenatal sSMC(15) cases with mosaic maternal inheritance.
Rui-Zhi Liu
exaly +5 more sources
Small supernumerary marker chromosomes (sSMCs) are structurally abnormal chromosomes that cannot be characterized by karyotype. In many prenatal cases of de novo sSMC, the outcome of pregnancy is difficult to predict because the euchromatin content is ...
Sébastien Jacquemont +2 more
exaly +5 more sources
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Characterization of sSMC by FISH and molecular techniques
European Journal of Medical Genetics, 2011Small supernumerary marker chromosome (sSMC) is a structurally altered additional chromosome that may not be explicitly clarified by conventional karyotyping alone. About one third of sSMC carriers have abnormal phenotypes and its clinical correlation is difficult, especially in prenatal studies.
Frenny Sheth +2 more
exaly +4 more sources
sSMC Characterization in a Male with Turner Syndrome Stigmata
Background: Small supernumerary marker chromosomes (sSMC) are rare cytogenetic findings in general, but especially in Turner syndrome so called sSMC<sup>T</sup> in a karyotype 46, X, +mar are even more scarce. According to the literature, sSMC<sup>T</sup> are derived from one of the Y-chromosomes in ~70% of the cases.
Thomas Liehr, Kristin Mrasek
exaly +2 more sources
Prenatal Diagnosis, 2007
AbstractA prenatally ascertained case with a de novo small supernumerary marker chromosome (sSMC) derived from chromosome 1 is reported. Due to a fetal heart defect the parents decided in favour of an induced abortion. Postmortem, a molecular cytogenetic study on eleven formalin fixed, paraffin‐embedded tissues of the fetus was performed, to further ...
Neil J. Sebire +2 more
exaly +3 more sources
AbstractA prenatally ascertained case with a de novo small supernumerary marker chromosome (sSMC) derived from chromosome 1 is reported. Due to a fetal heart defect the parents decided in favour of an induced abortion. Postmortem, a molecular cytogenetic study on eleven formalin fixed, paraffin‐embedded tissues of the fetus was performed, to further ...
Neil J. Sebire +2 more
exaly +3 more sources
American Journal of Medical Genetics Part A, 2005
AbstractSmall supernumerary marker chromosomes (sSMC) in human are defined as additional centric derivatives smaller than chromosome 20. In the majority of the cases only one sSMC is present, leading to a more or less stable karyotype of 47,XX,+mar or 47,XY,+mar.
Thomas, Liehr +5 more
openaire +2 more sources
AbstractSmall supernumerary marker chromosomes (sSMC) in human are defined as additional centric derivatives smaller than chromosome 20. In the majority of the cases only one sSMC is present, leading to a more or less stable karyotype of 47,XX,+mar or 47,XY,+mar.
Thomas, Liehr +5 more
openaire +2 more sources
Small supernumerary marker chromosomes (sSMC) in humans
Cytogenetic and Genome Research, 2004Small supernumerary marker chromosomes (sSMC), defined as additional centric chromosome fragments too small to be identified or characterized unambiguously by banding cytogenetics alone, are present in 0.043% of newborn children. Several attempts have been made to correlate certain sSMC with a specific clinical picture, resulting in the description of ...
T, Liehr, U, Claussen, H, Starke
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$$\zeta $$-Ricci Soliton on Real Hypersurfaces of Nearly Kaehler 6-Sphere with SSMC
Mediterranean Journal of Mathematics, 2021zbMATH Open Web Interface contents unavailable due to conflicting licenses.
Pooja Bansal +2 more
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