Familial occurrence of a del(Xp-) chromosome: pitfall in karyotype/phenotype correlation
Am J Med Genet
.
1998 Dec 4;80(4):436-8.
doi: 10.1002/(sici)1096-8628(19981204)80:4<436::aid-ajmg26>3.0.co;2-4.
Authors
A Soyke
,
M Stumm
,
P Krebs
,
D U Kloos
,
P Wieacker
,
K Mohnike
,
J Elsner
PMID:
9856579
DOI:
10.1002/(sici)1096-8628(19981204)80:4<436::aid-ajmg26>3.0.co;2-4
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Adolescent
Adult
Child
Chromosome Deletion*
Family Health
Female
Humans
Karyotyping
Male
Pedigree
Phenotype
Turner Syndrome / genetics
Turner Syndrome / pathology
X Chromosome / genetics*