| Alternate, adjacent 2 and 3:1 meiotic segregation products from a balanced t(13;18) (q12;q11) carrier. | |
| | |
MedLine Citation:
|
PMID: 8261649 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
|
We present a case in which alternate, adjacent 2 and 3:1 meiotic segregations have occurred in the pregnancies of a female carrier of a balanced reciprocal translocation -46,XX,t(13;18) (q12;q11). Products of five conceptions effectively showed trisomy 18q, trisomy 18p or monosomy 18p. This is one of the rare rearrangements which can give rise to a variety of segregation modes including adjacent 2. |
| | |
Authors:
|
C Cotton; M Cummins; A Smith |
Related Documents
:
|
20666959 - Case of prenatally diagnosed non-mosaic trisomy 20 with minor abnormalities. 8240689 - Changing dysmorphology of trisomy 18 during midtrimester. 12224069 - Optimising the timing for nuchal translucency measurement. 7241529 - Familial chromosome translocation t(3;18)(p21;p11). 19813209 - Study on the applicability of frontomaxillary facial angle in the first-trimester triso... 15298979 - Embryo loss pattern is predominant in miscarriages with normal chromosome karyotype amo... 20615129 - Increased postpartum thyroxine replacement in hashimoto's thyroiditis. 9166359 - A critical review of the relationship between gestational weight gain and preterm deliv... 12346689 - Judgment, 25 february 1986. |
Publication Detail:
|
Type: Case Reports; Journal Article |
Journal Detail:
|
Title: Clinical genetics Volume: 44 ISSN: 0009-9163 ISO Abbreviation: Clin. Genet. Publication Date: 1993 Oct |
Date Detail:
|
Created Date: 1994-01-27 Completed Date: 1994-01-27 Revised Date: 2004-11-17 |
Medline Journal Info:
|
Nlm Unique ID: 0253664 Medline TA: Clin Genet Country: DENMARK |
Other Details:
|
Languages: eng Pagination: 193-5 Citation Subset: IM |
Affiliation:
|
Department of Genetics, Children's Hospital, Camperdown, NSW, Australia. |
Export Citation:
|
APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
|
Chromosomes, Human, Pair 13* Chromosomes, Human, Pair 18* Female Heterozygote Humans Infant, Newborn Karyotyping Male Meiosis Monosomy* Pedigree Pregnancy Translocation, Genetic* Trisomy* |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Previous Document: Oral-facial-digital syndrome with fibular aplasia: a new variant.
Next Document: The Myhre syndrome: report of two cases.