Review
doi: 10.1136/jmg.2.2.142.
KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS
- PMID: 14295659
- PMCID: PMC1012851
- DOI: 10.1136/jmg.2.2.142
Item in Clipboard
Review
KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS
J Med Genet.
1965 Jun.
No abstract available
Similar articles
-
[STUDY OF THE KARYOTYPE IN SOME TYPES OF GONADAL DYSGENESIS].An Fac Med Univ Repub Montev Urug. 1964;49:411-6. An Fac Med Univ Repub Montev Urug. 1964. PMID: 14290777 Spanish. No abstract available.
-
[A CASE OF GONADAL DYSGENESIS WITH CLITORIS ENLARGEMENT IN A PATIENT WITH A 45-XO KARYOTYPE].Endokrynol Pol. 1964 Nov-Dec;15:579-86. Endokrynol Pol. 1964. PMID: 14318604 Polish. No abstract available.
-
An isodicentric X chromosome with gonadal dysgenesis in a lady without prominent somatic features of Turner's syndrome. A case report.J Formos Med Assoc. 2015 Jan;114(1):77-80. doi: 10.1016/j.jfma.2011.05.011. Epub 2012 May 2. J Formos Med Assoc. 2015. PMID: 25618587
-
A CASE OF GONADAL DYSGENESIS WITH PHALLIC ENLARGEMENT AND A 45/XO KARYOTYPE.Acta Obstet Gynecol Scand. 1964;43:255-61. doi: 10.3109/00016346409157931. Acta Obstet Gynecol Scand. 1964. PMID: 14248207 No abstract available.
-
[A CASE OF BONNEVIE-ULRICH-TURNER SYNDROME WITH GONADAL DYSGENESIS AND KARYOTYPE 45/XO].Rev Esp Pediatr. 1964 Jan-Feb;20:79-88. Rev Esp Pediatr. 1964. PMID: 14154094 Spanish. No abstract available.
Cited by
-
Duchenne muscular dystrophy due to familial Xp21 deletion detectable by DNA analysis and flow cytometry.Hum Genet. 1986 Jun;73(2):175-80. doi: 10.1007/BF00291610. Hum Genet. 1986. PMID: 3721503
-
Late-replicating ring X-chromosomes identified by R-banding after BrdU pulse. Three new examples of mosaicism 45, XO/46, Xr(X).Hum Genet. 1976 Sep 10;34(1):45-52. doi: 10.1007/BF00284433. Hum Genet. 1976. PMID: 61162
-
[Karyotype-phenotype correlation in a 46,Xdel(X) (p22) diagnosis (author's transl)].Hum Genet. 1976 Mar 12;31(3):263-70. doi: 10.1007/BF00270856. Hum Genet. 1976. PMID: 955625 German.
-
[The nosologic place of the XO-XY mosaicism].Arch Gynakol. 1968;206(4):369-410. doi: 10.1007/BF00668069. Arch Gynakol. 1968. PMID: 4893320 Review. German. No abstract available.
-
Human X-autosome translocations: differential inactivation of the X chromosome in a kindred with an X-9 translocation.Am J Hum Genet. 1975 Jul;27(4):441-53. Am J Hum Genet. 1975. PMID: 1155455 Free PMC article.
References
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources