doi: 10.1007/BF00283989.
A case of the 18p--syndrome
- PMID: 4641844
- DOI: 10.1007/BF00283989
Item in Clipboard
A case of the 18p--syndrome
Humangenetik.
1972.
No abstract available
Similar articles
-
[E 18 ring chromosome--case report and review].Klin Padiatr. 1972 Nov;184(6):495-500. Klin Padiatr. 1972. PMID: 4675258 German. No abstract available.
-
[The clinical features of the 18 q-syndrome (author's transl)].Wien Klin Wochenschr. 1974 Aug 16;86(15):441-4. Wien Klin Wochenschr. 1974. PMID: 4605988 German. No abstract available.
-
[Morphologic abnormality due to duplication of chromosome 17 (46,XY,17q+) in a newborn infant].Union Med Can. 1974 Aug;103(8):1404-8. Union Med Can. 1974. PMID: 4849205 French. No abstract available.
-
[Ring chromosome 18. 18p-/18q- -deletion-syndrome].Humangenetik. 1972;15(4):289-318. doi: 10.1007/BF00281730. Humangenetik. 1972. PMID: 4565746 Review. German. No abstract available.
-
[Eye anomalies in chromosomal aberrations].Oftalmol Zh. 1971;26(4):299-306. Oftalmol Zh. 1971. PMID: 4256612 Review. Russian. No abstract available.
Cited by
-
Heart disease associated with deletion of the short arm of chromosome 18.Pediatr Cardiol. 1989 Summer;10(3):174-6. doi: 10.1007/BF02081684. Pediatr Cardiol. 1989. PMID: 2678018 Review.