doi: 10.1111/j.1399-0004.1975.tb00355.x.
49, XXXXY patient with hemifacial microsomia
- PMID: 1149315
- DOI: 10.1111/j.1399-0004.1975.tb00355.x
Item in Clipboard
49, XXXXY patient with hemifacial microsomia
Clin Genet.
1975 May-Jun.
No abstract available
Similar articles
-
49,XXXXY: a distinct phenotype. Three new cases and review.J Med Genet. 1998 May;35(5):420-4. doi: 10.1136/jmg.35.5.420. J Med Genet. 1998. PMID: 9610808 Free PMC article.
-
Hemifacial microsomia.Am J Dis Child. 1971 Jul;122(1):57-8. Am J Dis Child. 1971. PMID: 4998565 No abstract available.
-
49, XXXXY syndrome with severe vesico-ureteral reflux and hydronephrosis: report of one case.Acta Paediatr Taiwan. 2005 Jan-Feb;46(1):35-8. Acta Paediatr Taiwan. 2005. PMID: 16302576
-
Rare sex chromosome aneuploidies in humans: report of six patients with 48,XXYY, 49,XXXXY, and 48,XXXX karyotypes.Am J Med Genet. 1999 Jul 2;85(1):86-7. doi: 10.1002/(sici)1096-8628(19990702)85:1<86::aid-ajmg16>3.0.co;2-m. Am J Med Genet. 1999. PMID: 10377019 Review. No abstract available.
-
Sex chromosome disorders.Crit Rev Clin Lab Sci. 1981;13(4):241-82. doi: 10.3109/10408368109106449. Crit Rev Clin Lab Sci. 1981. PMID: 7016435 Review.
Cited by
-
49,XXXXY: a distinct phenotype. Three new cases and review.J Med Genet. 1998 May;35(5):420-4. doi: 10.1136/jmg.35.5.420. J Med Genet. 1998. PMID: 9610808 Free PMC article.
-
Prevalence, prenatal diagnosis and clinical features of oculo-auriculo-vertebral spectrum: a registry-based study in Europe.Eur J Hum Genet. 2014 Aug;22(8):1026-33. doi: 10.1038/ejhg.2013.287. Epub 2014 Jan 8. Eur J Hum Genet. 2014. PMID: 24398798 Free PMC article.
MeSH terms
LinkOut - more resources
Full Text Sources
