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Parent Perspectives of Support Received from Physicians and/or Genetic Counselors Following a Decision to Continue a Pregnancy with a Prenatal Diagnosis of Trisomy 13/18.
Published in:
Journal of Genetic Counseling, 2018, v. 27, n. 3, p. 656, doi. 10.1007/s10897-017-0168-6
By:
- Wallace, Stephanie E.;
- Gilvary, Sara;
- Smith, Michael J.;
- Dolan, Siobhan M.
Publication type:
Article
Impact of preoperative screening for rectal colonization with fluoroquinolone-resistant enteric bacteria on the incidence of sepsis following transrectal ultrasound guided prostate biopsy.
Published in:
Research & Reports in Urology, 2017, v. 9, p. 37, doi. 10.2147/RRU.S117206
By:
- Farrell, John J.;
- Hicks, Jennifer L.;
- Wallace, Stephanie E.;
- Seftel, Allen D.
Publication type:
Article
Recessive mutations in VPS13D cause childhood onset movement disorders.
Published in:
2018
By:
- Gauthier, Julie;
- Meijer, Inge A.;
- Lessel, Davor;
- Mencacci, Niccolò E.;
- Krainc, Dimitri;
- Hempel, Maja;
- Tsiakas, Konstantinos;
- Prokisch, Holger;
- Rossignol, Elsa;
- Helm, Margaret H.;
- Rodan, Lance H.;
- Karamchandani, Jason;
- Carecchio, Miryam;
- Lubbe, Steven J.;
- Telegrafi, Aida;
- Henderson, Lindsay B.;
- Lorenzo, Kerry;
- Wallace, Stephanie E.;
- Glass, Ian A.;
- Hamdan, Fadi F.
Publication type:
journal article
Recurrent HERV- H-Mediated 3q13.2-q13.31 Deletions Cause a Syndrome of Hypotonia and Motor, Language, and Cognitive Delays.
Published in:
Human Mutation, 2013, v. 34, n. 10, p. 1415, doi. 10.1002/humu.22384
By:
- Shuvarikov, Andrey;
- Campbell, Ian M.;
- Dittwald, Piotr;
- Neill, Nicholas J.;
- Bialer, Martin G.;
- Moore, Christine;
- Wheeler, Patricia G.;
- Wallace, Stephanie E.;
- Hannibal, Mark C.;
- Murray, Michael F.;
- Giovanni, Monica A.;
- Terespolsky, Deborah;
- Sodhi, Sandi;
- Cassina, Matteo;
- Viskochil, David;
- Moghaddam, Billur;
- Herman, Kristin;
- Brown, Chester W.;
- Beck, Christine R.;
- Gambin, Anna
Publication type:
Article
Improving the Value of Costly Genetic Reference Laboratory Testing With Active Utilization Management.
Published in:
Archives of Pathology & Laboratory Medicine, 2014, v. 138, n. 1, p. 110, doi. 10.5858/arpa.2012-0726-OA
By:
- Dickerson, Jane A.;
- Cole, Bonnie;
- Conta, Jessie H.;
- Wellner, Monica;
- Wallace, Stephanie E.;
- Jack, Rhona M.;
- Rutledge, Joe;
- Astion, Michael L.
Publication type:
Article

Found: 5

Parent Perspectives of Support Received from Physicians and/or Genetic Counselors Following a Decision to Continue a Pregnancy with a Prenatal Diagnosis of Trisomy 13/18.

Impact of preoperative screening for rectal colonization with fluoroquinolone-resistant enteric bacteria on the incidence of sepsis following transrectal ultrasound guided prostate biopsy.

Recessive mutations in VPS13D cause childhood onset movement disorders.

Recurrent HERV- H-Mediated 3q13.2-q13.31 Deletions Cause a Syndrome of Hypotonia and Motor, Language, and Cognitive Delays.

Improving the Value of Costly Genetic Reference Laboratory Testing With Active Utilization Management.