Inv(4)(p16q21). A five-generation pedigree with 24 carriers and no recombin ants
- 1 February 1987
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 31 (2) , 97-101
- https://doi.org/10.1111/j.1399-0004.1987.tb02776.x
Abstract
A familial inv(4)(p16q21) ascertained through a woman who had a thanatophoric dwarf daughter and two abortions is presented. She and 23 other relatives were carriers, but no recombinants were found. The proportion of abortions and neonatal deaths in carriers' offspring was similar to that in non‐carriers. A random segregation of the inverted chromosome was observed. The analysis of the present and previous familial chromosome 4 pericentric inversions indicates that: a) the breakpoint in q, with a limit between q21 and q25 determines the occurrence of inherited unbalances, and b) most recombinant chromosomes have duplication of the larger distal segment.Keywords
This publication has 11 references indexed in Scilit:
- Familial pericentric inversion of chromosome 19, inv(19) (p13q13) with a note on genetic counseling of pericentric inversion carriersClinical Genetics, 2008
- The critical monosomic segment involved in 4p- syndrome: A high-resolution banding study on five inherited casesJournal of Human Genetics, 1984
- Pericentric inversionsHuman Genetics, 1984
- A homozygote for pericentric inversion of chromosome 4.Journal of Medical Genetics, 1982
- Study on segregation of the inversion of chromosome 4 (p15.2q11) in two unrelated familiesHuman Genetics, 1982
- Structural differences in pericentric inversions. Application to a model of risk of recombinantsHuman Genetics, 1981
- Pericentric inversion of chromosome 14 and the risk of partial duplication of 14q (14q31 → 14qter)American Journal of Medical Genetics, 1977
- Pericentric inversion and partial monosomy 4q associated with congenital anomaliesHuman Genetics, 1977
- Cytological assessment of meiotic exchange in a human male with a pericentric inversion of chromosome No. 4Cytogenetic and Genome Research, 1975
- Multiple congenital anomaliesassociated with probable pericentric inversion of chromosome No. 4 and mosaicism in an asymptomatic motherThe Journal of Pediatrics, 1964