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Keyword Connections - mosaicism Keywords

Connection Type	Connection
Journals	Cureus Frontiers in endocrinology molecular therapy methods & clinical development European journal of medical genetics reproductive biomedicine online Annals of hematology
Research Groups	No Research Group Connected
Bibliographies	[1] Clinical outcomes after the transfer of blastocysts characterized as mosaic by high resolution Next Generation Sequencing- further insights. [2] Controversies in ART: can the IVF laboratory influence preimplantation embryo aneuploidy? [3] Mosaicism in Fanconi anemia: concise review and evaluation of published cases with focus on clinical course of blood count normalization. [4] Novel Variants and Mosaicism in Pompe Disease Identified by Extended Analyses of Patients with an Incomplete DNA Diagnosis. [5] implications of aneuploidy for stem cell biology and brain therapeutics [6] mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: prenatal diagnosis, molecular cytogenetic characterization, and association with 2-mb deletion of 21q21.1–q21.2 and 5-mb deletion of 21q22.3 [7] prenatal diagnosis and genetic analysis of a fetus with 47,xx, +21/46,xx mosaicism and xx/xy chimerism [8] mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses [9] prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21 [10] mosaicismo inusual en un caso de diagnóstico prenatal citogenético [11] Frequency of variants and parental mosaicism in families with inactivating PTH/PTHrP signaling disorder type 2. [12] Testing With Intent in Mosaic Conditions: A Case-Based Review. [13] Short Stature on a Boy: Mosaicism with an Isodicentric Y Chromosome [14] A novel KRT86 mutation in a Turkish family with monilethrix, and identification of maternal mosaicism. [15] Degree of mosaicism in trophectoderm does not predict pregnancy potential: a corrected analysis of pregnancy outcomes following transfer of mosaic embryos [16] Postzygotic mosaicism in basal cell naevus syndrome. [17] Mosaicism in Fanconi anemia: concise review and evaluation of published cases with focus on clinical course of blood count normalization. [18] Novel Variants and Mosaicism in Pompe Disease Identified by Extended Analyses of Patients with an Incomplete DNA Diagnosis. [19] a newborn with genital ambiguity, 45,x/46,xy mosaicism, a jumping chromosome y, and congenital adrenal hyperplasia [20] prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome [21] prenatal diagnosis and genetic analysis of a fetus with 47,xx, +21/46,xx mosaicism and xx/xy chimerism [22] prenatal diagnosis of low-level mosaicism for trisomy 21 with rare karyotype detected by noninvasive prenatal testing [23] a rare inherited 15q11.2-q13.1 interstitial duplication with maternal somatic mosaicism, renal carcinoma and autism [24] prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21 [25] mosaicismo inusual en un caso de diagnóstico prenatal citogenético [26] Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE) [27] Frequency of variants and parental mosaicism in families with inactivating PTH/PTHrP signaling disorder type 2.