doi: 10.1136/jmg.8.3.381.
An extra small metacentric chromosome in association with multiple congenital abnormalities
- PMID: 5097148
- PMCID: PMC1469157
- DOI: 10.1136/jmg.8.3.381
Item in Clipboard
An extra small metacentric chromosome in association with multiple congenital abnormalities
J Med Genet.
1971 Sep.
No abstract available
Similar articles
-
An extra small metacentric chromosome in a mentally retarded boy.J Med Genet. 1968 Dec;5(4):335-40. doi: 10.1136/jmg.5.4.335. J Med Genet. 1968. PMID: 5713650 Free PMC article. No abstract available.
-
An extra small metacentric autosome in a mentally retarded boy with multiple malformations.J Med Genet. 1971 Sep;8(3):378-80. doi: 10.1136/jmg.8.3.378. J Med Genet. 1971. PMID: 5097147 Free PMC article. No abstract available.
-
Tertiary trisomy in a human kindred containing an E/G translocation.Am J Hum Genet. 1971 Sep;23(5):431-41. Am J Hum Genet. 1971. PMID: 5092595 Free PMC article. No abstract available.
-
Autosomal chromosome aberrations in ophthalmology.Int Ophthalmol Clin. 1968 Winter;8(4):839-910. Int Ophthalmol Clin. 1968. PMID: 4244691 Review. No abstract available.
-
[Autosomal chromosome aberrations].Arch Genet (Zur). 1979;52(1-2):1-204. Arch Genet (Zur). 1979. PMID: 389192 Review. German. No abstract available.
Cited by
-
Multiple anomalies associated with an extra small metacentric chromosome: modified Giemsa stain results.Humangenetik. 1973;18(4):291-5. doi: 10.1007/BF00291125. Humangenetik. 1973. PMID: 4125989 No abstract available.
-
A case of hypogonadotrophic hypogonadism with anosmia (Kallmann's syndrome) in a male, with familial incidence of a small metacentric chromosome (47,XX, mat?+).J Med Genet. 1976 Feb;13(1):71-5. doi: 10.1136/jmg.13.1.71. J Med Genet. 1976. PMID: 1271431 Free PMC article.
-
Significance of detection of extra metacentric microchromosome in amniotic cell culture.J Med Genet. 1978 Apr;15(2):136-42. doi: 10.1136/jmg.15.2.136. J Med Genet. 1978. PMID: 641948 Free PMC article.
-
Small metacentric nonsatellited extra chromosome: report of five mentally retarded individuals and review of literature. Contribution to further delineation of a new syndrome.Hum Genet. 1978 Oct 19;44(1):59-69. doi: 10.1007/BF00283575. Hum Genet. 1978. PMID: 711239
-
[Cat-eye syndrome. Clinical and cytogenetical differentialdiagnosis (author's transl)].Humangenetik. 1975;26(4):271-89. Humangenetik. 1975. PMID: 50268 Review. German.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
