doi: 10.1007/BF00394195.
Trisomy 4p14 leads to 4pter with translocation t(4;15)(p14;p12) in the father
- PMID: 1176148
- DOI: 10.1007/BF00394195
Item in Clipboard
Trisomy 4p14 leads to 4pter with translocation t(4;15)(p14;p12) in the father
Humangenetik.
.
Abstract
A trisomy 4p14 leads to 4pter in a 15-year-old girl is reported. The main features are physical and mental retardation and the absence of gross malformations. The relevance of other symptoms found in the patient is discussed.
Similar articles
-
Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).Humangenetik. 1975 Dec 23;30(4):307-16. doi: 10.1007/BF00275143. Humangenetik. 1975. PMID: 1218860
-
A complex four-break rearrangement between chromosomes 4 and 13 resulting in a recombinant chromosome 4.Cytogenet Cell Genet. 1981;30(1):3-10. doi: 10.1159/000131581. Cytogenet Cell Genet. 1981. PMID: 7261680
-
A 6p trisomy detected in a family with a "giant satellite".Humangenetik. 1975 Oct 20;30(1):63-7. doi: 10.1007/BF00273632. Humangenetik. 1975. PMID: 1184005
-
Trisomy 4q syndrome: presentation of a new case and review of the literature.Ann Genet. 2002 Apr-Jun;45(2):53-7. doi: 10.1016/s0003-3995(02)01117-6. Ann Genet. 2002. PMID: 12119211 Review.
-
Reproductive possibilities for balanced translocation (14) carriers in families with partial trisomy of proximal 14q.J Med Genet. 1993 Jan;30(1):73-5. doi: 10.1136/jmg.30.1.73. J Med Genet. 1993. PMID: 8423613 Free PMC article. Review.
Cited by
-
Clinical manifestations of trisomy 4p syndrome.Eur J Pediatr. 1995 Jun;154(6):425-31. doi: 10.1007/BF02029349. Eur J Pediatr. 1995. PMID: 7671938 Review.
-
Two cases of trisomy 4p with translocation t(4p-,7q+) in several members of one family.Hum Genet. 1976 Jul 27;33(2):155-60. doi: 10.1007/BF00281889. Hum Genet. 1976. PMID: 939567
-
Trisomy 4p due to a paternal t(4p-;16p+) translocation.Hum Genet. 1976 Oct 28;34(2):227-30. doi: 10.1007/BF00278894. Hum Genet. 1976. PMID: 1002146
-
Hand dermatoglyphics in trisomy 4p.Hum Genet. 1976 Dec 15;34(3):271-6. doi: 10.1007/BF00295290. Hum Genet. 1976. PMID: 1002150
References
MeSH terms
LinkOut - more resources
Research Materials