Case Reports
doi: 10.1007/BF00393617.
Deletion long arm 13
- PMID: 885554
- DOI: 10.1007/BF00393617
Item in Clipboard
Case Reports
Deletion long arm 13
Hum Genet.
.
No abstract available
Similar articles
-
Inherited partial duplication of chromosome No. 15.J Med Genet. 1974 Sep;11(3):287-91. doi: 10.1136/jmg.11.3.287. J Med Genet. 1974. PMID: 4139262 Free PMC article.
-
Microcephaly, mental retardation and hypertelorism in chromosome deletion studies.Neurology. 1973 Nov;23(11):1141-6. doi: 10.1212/wnl.23.11.1141. Neurology. 1973. PMID: 4795737 No abstract available.
-
Retinoblastoma and deletion D (14) syndrome.J Med Genet. 1969 Sep;6(3):322-7. doi: 10.1136/jmg.6.3.322. J Med Genet. 1969. PMID: 5345106 Free PMC article. No abstract available.
-
Developmental abnormalities associated with a ring chromosome 6.J Med Genet. 1973 Sep;10(3):299-303. doi: 10.1136/jmg.10.3.299. J Med Genet. 1973. PMID: 4774541 Free PMC article.
-
Comparative behavior of ring chromosomes.Am J Hum Genet. 1970 May;22(3):304-18. Am J Hum Genet. 1970. PMID: 5445002 Free PMC article. No abstract available.
Cited by
-
Interstitial deletion of chromosome 13: prognosis and adult phenotype.J Med Genet. 1991 Aug;28(8):533-5. doi: 10.1136/jmg.28.8.533. J Med Genet. 1991. PMID: 1920369 Free PMC article.
-
Interstitial deletion 13q syndromes: a report on two unrelated patients.Hum Genet. 1979;52(3):269-74. doi: 10.1007/BF00278676. Hum Genet. 1979. PMID: 535887
-
Deletion of band 13q21 is compatible with normal phenotype.Hum Genet. 1985;70(1):87-91. doi: 10.1007/BF00389468. Hum Genet. 1985. PMID: 3997156
-
Interstitial del(13)(q21.3q31) associated with psychomotor retardation, eczema, and absent suck and swallowing reflex.J Med Genet. 1987 Dec;24(12):786-8. doi: 10.1136/jmg.24.12.786. J Med Genet. 1987. PMID: 3430559 Free PMC article.
-
Retinoblastoma: host resistance and 13q- chromosomal deletion.Hum Genet. 1980;56(1):53-8. doi: 10.1007/BF00281568. Hum Genet. 1980. PMID: 7203480