• 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes
• 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes
• A case of partial trisomy 15q25.3-qter
• A female infant with duplication of chromosome 2q33 to 2q37.3
• Case report of newborn with de novo partial trisomy 2q31.2-37.3 and monosomy 9p24.3
• Cryptic subtelomeric translocation t(2;16)(q37;q24) segregating in a family with unexplained stillbirths and a dysmorphic, slightly retarded child
• Duplication 2q33 leads to 2q37 due to paternal ins (12;2) translocation
• Duplication of the ZIC2 gene is not associated with holoprosencephaly
• Effective monosomy or trisomy of chromosome band 2q37.3 due to the unbalanced segregation of a 2;11 translocation
• Exome and genome sequencing to unravel the precise breakpoints of partial trisomy 6q and partial Monosomy 2q
• Familial cryptic translocation (2;17) ascertained through recurrent spontaneous abortions
• Heterogeneity of a Constitutional Complex Chromosomal Rearrangement in 2q
• Joubert syndrome co-existing with partial Xp trisomy: review of the literature
• Partial trisomy 2q(2q37.3-->qter) and monosomy 7q(7q34--->qter) due to paternal reciprocal translocation 2;7: a case report
• Partial trisomy 2q(2q37.3-->qter) and monosomy 7q(7q34--->qter) due to paternal reciprocal translocation 2;7: a case report
• Prenatal Diagnosis and Molecular Cytogenetic Characterization of Copy Number Variations on 4p15.2p16.3, Xp22.31, and 12p11.1q11 in a Fetus with Ultrasound Anomalies: A Case Report and Literature Review
• Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly
• Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results
• Prenatal diagnosis of partial monosomy 2q (2q37.3qter) and partial trisomy 10q (10q24.31qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results