doi: 10.1001/archpedi.1972.02110180110016.
An 18p21q translocation in a patient with presumptive "monosomy G"
- PMID: 4639227
- DOI: 10.1001/archpedi.1972.02110180110016
Item in Clipboard
An 18p21q translocation in a patient with presumptive "monosomy G"
Am J Dis Child.
1972 Dec.
No abstract available
Similar articles
-
A case of a girl with a 21 ring chromosome.Hum Hered. 1974;24(1):100-4. doi: 10.1159/000152643. Hum Hered. 1974. PMID: 4136482 No abstract available.
-
Identification of 21r and 22r chromosomes by quinacrine fluorescence.Clin Genet. 1972;3(4):264-70. doi: 10.1111/j.1399-0004.1972.tb04275.x. Clin Genet. 1972. PMID: 5054320 No abstract available.
-
Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+).Cytogenetics. 1971;10(6):413-26. doi: 10.1159/000130162. Cytogenetics. 1971. PMID: 5146418 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.
-
An etiologic and nosologic overview of craniosynostosis syndromes.Birth Defects Orig Artic Ser. 1975;11(2):137-89. Birth Defects Orig Artic Ser. 1975. PMID: 179637 Review.
Cited by
-
A 46,XY, del(18)(pter leads to p1 100:) cebocephalic child from a 46,XX,t(12;18)(18pter leads to 18 p 1100:: 12qter leads to 12pter) normal parent.Hum Genet. 1976 Sep 10;34(1):103-6. doi: 10.1007/BF00284446. Hum Genet. 1976. PMID: 964998
-
An inherited small extra chromosome: a mother with 46,XX,t(17;22)(pl;ql) and a son with 47,XY,+der(22)mat.J Med Genet. 1973 Dec;10(4):379-84. doi: 10.1136/jmg.10.4.379. J Med Genet. 1973. PMID: 4129973 Free PMC article.
-
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.
-
A male infant with monosomy 21.Humangenetik. 1975 Aug 29;29(1):1-7. doi: 10.1007/BF00273344. Humangenetik. 1975. PMID: 1176129
-
Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region.Am J Hum Genet. 1995 Jul;57(1):62-71. Am J Hum Genet. 1995. PMID: 7611297 Free PMC article.