PMID- 9297507 OWN - NLM STAT- MEDLINE DCOM- 19980211 LR - 20190831 IS - 0009-5915 (Print) IS - 0009-5915 (Linking) VI - 106 IP - 5 DP - 1997 Oct TI - Sequential immunocytogenetics, molecular cytogenetics and transmission electron microscopy of microspread meiosis I oocytes from a human fetal carrier of an unbalanced translocation. PG - 293-303 AB - The oocytes of a 17 week human fetus carrying an unbalanced 46,XX, add(18)(p13) translocation were studied with a sequential combination of microspreading, immunocytogenetics, fluorescence in situ hybridization (FISH) and transmission electron microscopy. This combination of technologies allowed the collection of data of unique accuracy and resolution. The translocated chromosome was found to be involved in five different synaptic configurations. A consistent feature of these configurations was the involvement of a second small bivalent, presumably chromosome 21 or 22, the normal synapsis of which was often disrupted. We conclude that chromosome 21 or 22 was the source of the translocated material, which was found to be either homologously triply synapsed, heterologously synapsed or asynapsed. FAU - Barlow, A L AU - Barlow AL AD - LSF Research Unit, Regional Genetics Services, Heartlands Hospital, Yardley Green Road, Birmingham B9 5PX, UK. FAU - Hulten, M A AU - Hulten MA LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - Austria TA - Chromosoma JT - Chromosoma JID - 2985138R SB - IM MH - Adult MH - Chromosomes, Human, Pair 18 MH - Cytogenetics/*methods MH - Embryo, Mammalian/physiology MH - Female MH - Humans MH - In Situ Hybridization, Fluorescence/methods MH - *Meiosis MH - Microscopy, Electron MH - Oocytes/*physiology MH - Pregnancy MH - *Translocation, Genetic EDAT- 1997/09/23 00:00 MHDA- 1997/09/23 00:01 CRDT- 1997/09/23 00:00 PHST- 1997/09/23 00:00 [pubmed] PHST- 1997/09/23 00:01 [medline] PHST- 1997/09/23 00:00 [entrez] AID - 10.1007/s004120050250 [doi] PST - ppublish SO - Chromosoma. 1997 Oct;106(5):293-303. doi: 10.1007/s004120050250.