skip to main content
Guest
My Research
My Account
Sign out
Sign in
This feature requires javascript
Library Search
Find Databases
Browse Search
E-Journals A-Z
E-Books A-Z
Citation Linker
Help
Language:
English
Vietnamese
This feature required javascript
This feature requires javascript
Primo Search
All Library Resources
All
Course Materials
Course Materials
Search For:
Clear Search Box
Search in:
All Library Resources
Or hit Enter to replace search target
Or select another collection:
Search in:
All Library Resources
Search in:
Print Resources
Search in:
Digital Resources
Search in:
Online E-Resources
Advanced Search
Browse Search
This feature requires javascript
Search Limited to:
Search Limited to:
Resource type
criteria input
All items
Books
Articles
Images
Audio Visual
Maps
Graduate theses
Show Results with:
criteria input
that contain my query words
with my exact phrase
starts with
Show Results with:
Search type Index
criteria input
anywhere in the record
in the title
as author/creator
in subject
Full Text
ISBN
ISSN
TOC
Keyword
Field
Show Results with:
in the title
Show Results with:
anywhere in the record
in the title
as author/creator
in subject
Full Text
ISBN
ISSN
TOC
Keyword
Field
This feature requires javascript
Triploidy syndrome: A report on two live-born (69, XXY) and one still-born (69, XXX) infants
Clinical genetics, 1976-01, Vol.9 (1), p.43-50
[Peer Reviewed Journal]
ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1976.tb01548.x ;PMID: 174849
Full text available
Citations
Cited by
View Online
Details
Recommendations
Reviews
Times Cited
External Links
This feature requires javascript
Actions
Add to My Research
Remove from My Research
E-mail
Print
Permalink
Citation
EasyBib
EndNote
RefWorks
Delicious
Export RIS
Export BibTeX
This feature requires javascript
Title:
Triploidy syndrome: A report on two live-born (69, XXY) and one still-born (69, XXX) infants
Author:
Saadi, A. Al
;
Juliar, Joseph F.
;
Harm, John
;
Brough, A. Joseph
;
Perrin, Eugene v.
;
Chen, Harold
Subjects:
Abnormalities, Multiple
;
Adrenal Glands - abnormalities
;
Chromosome Aberrations
;
Chromosome Disorders
;
Coloboma - genetics
;
Ear, External - abnormalities
;
Female
;
Genitalia, Male - abnormalities
;
Hand
;
Heart Defects, Congenital - genetics
;
Humans
;
Hypertelorism - genetics
;
Infant, Newborn
;
Karyotyping
;
Kidney - abnormalities
;
Male
;
Polyploidy
;
Syndactyly - genetics
;
Syndrome
Is Part Of:
Clinical genetics, 1976-01, Vol.9 (1), p.43-50
Description:
Two live‐born cases, 69, XXY and one stillbirth, 69, XXX are reported. Further evidence is presented to delineate the triploidy syndrome. Common external and internal features which characterize the triploidy syndrome are low‐set ears, hypertelorism, colobomata, syndactyly, simian creases, microphallus, undescended testes, scrotal aplasia, anomalous heart and hypoplasia of kidneys and adrenals. The triploidy syndrome encompasses features found in trisomies 13, 18 and 21. We suggest that the abnormal development of the triploidy infants is the result of the mentioned trisomies and their subsequent effect on the remaining genome.
Publisher:
Oxford, UK: Blackwell Publishing Ltd
Language:
English
Identifier:
ISSN: 0009-9163
EISSN: 1399-0004
DOI: 10.1111/j.1399-0004.1976.tb01548.x
PMID: 174849
Source:
MEDLINE
Alma/SFX Local Collection
This feature requires javascript
This feature requires javascript
Back to results list
Previous
Result
8
Next
This feature requires javascript
This feature requires javascript
Searching Remote Databases, Please Wait
Searching for
in
scope:(TDTS),scope:(SFX),scope:(TDT),scope:(SEN),primo_central_multiple_fe
Show me what you have so far
This feature requires javascript
This feature requires javascript