URGENT ARTICLE SEARCH!!!!

[sometime]

Dear all, I am a new member...I am desperately trying to find the PDF file with full text of the following article:

First-trimester genetic diagnosis: a series of six cases
South dacoda medicine 2010, Mar 63(3): 83-5
PMID 20301870
Stein QP et all

and any other article that can hepl to understand if after an ultrasound screen with biochemical marckers unusual and normal NT ( and combined risk normal) it is adviceble to go through amniocentesis or not!!

The university of the city where I live has no access to this review unfortunately!

[JackBean]

I'm little afraid that for articvle from South dacoda medicine you will have to contact the authors Our system doesn't even know that journal

[sometime]

WEll...I looked in pubmed but there is no e-mail address of the corresponding author unfortunately....the following is all it appears:

First-trimester genetic diagnosis: a series of six cases
S D Med. 2010 Mar;63(3):83-5.
First-trimester genetic diagnosis: a series of six cases.
Stein QP, Flanagan JD, Knutsen-Larson S, Van Eerden P.
Source

Sanford Women's Health & Sanford Children's Specialty Clinic, Sioux Falls, SD, USA.
Abstract

A first-trimester screen consists of a nuchal translucency (NT) ultrasound measurement as well as maternal serum testing for pregnancy-associated plasma protein-A (PAPP-A) and human chorionic gonadotropin (hCG). An increased nuchal translucency (NT) thickness at 11 to 14 weeks gestational age is a common finding for Down syndrome, Trisomy 18 and cardiac defects. We present a series of six patients, four with NT measurements greater than the 95th centile, and two additional cases where the NT was normal, but maternal serum biochemical markers were unusual. All six of these cases had a chromosome anomaly or another genetic condition: Noonan syndrome, triploidy, Down syndrome, Trisomy 18, Turner syndrome and a rare chromosome abnormality known as Ring 18-Monosomy 18. Our series underlines the fact that it is important to explore other genetic and chromosome abnormalities, in addition to Down syndrome and Trisomy 18, when there is an abnormality on a first-trimester screen.

PMID:
20301870
[PubMed - indexed for MEDLINE]

ANY OTHER IDEA??? (!!

[JackBean]

this is page of the clinic, where they (at least the first one) work http://www.sanfordhealth.org/Contact However, I cannot find contact directly to him, so try to write to the clinic for contact to the doctor and then...

[sometime]

thank you millions!!! ! Your suggestion helped me to find the address of Professor Stein and wrote him an e-mail for paper request...hoping that he'll reply!