| Literature DB >> 1773535 |
T Hasegawa1, Y Hasegawa, S Asamura, T Nagai, Y Tsuchiya, M Ninomiya, Y Fukushima.
Abstract
Familial cases (a grandfather, a father and a daughter) of the EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) are reported. All of them have a balanced reciprocal translocation (46,XY or XX, t(7;9) (q11.21;p12) or (46,XY or XX, t(7;9) (p11.2;q12)), but no other members of the family have either the EEC syndrome or chromosome abnormalities. This indicates that one of the chromosome sites 7q11.21, 9p12, 7p11.2 and 9q12 is a candidate for gene locus of the EEC syndrome.Entities:
Mesh:
Year: 1991 PMID: 1773535 DOI: 10.1111/j.1399-0004.1991.tb03077.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438