• Application of personal computer to an analysis of small de novo chromosomal insertion: a case of de novo 3q2 trisomy with ins(8;3)
• Clinical, Cytogenetic, and Biochemical Analyses of a Family with a t(3;13)(q26.2;p11.2): Further Delineation of 3q Duplication Syndrome
• Familial trisomy 3q25----qter. Report of two cases
• New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conception
• Partial duplication of 3q and distal deletion of 10q inherited from a maternal balanced translocation
• Partial trisomy 3q syndrome inherited from familial t(3;9)(q26.1; p23)
• Partial trisomy for the long arm of chromosome 3 [3(q21 to qter)+] in a newborn with minor physical stigmata
• Prenatal identification of partial 3q duplication syndrome
• Probing the human genome in search for a new 3q syndrome
• The structural gene for transferrin (TF) maps to 3q21----3qter
• Trisomy 3q2 and Pierre-Robin sequence in a boy with unbalanced 46,XY, der(10), t(3;10)(q23;q26.3) de novo karyotype