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Correction to: Talking with Children about Adult-Onset Hereditary Cancer Risk: A Developmental Approach for Parents.
Published in:
Journal of Genetic Counseling, 2018, v. 27, n. 6, p. 1523, doi. 10.1007/s10897-018-0282-0
By:
- Werner-Lin, Allison;
- Merrill, Shana L.;
- Brandt, Amanda C.;
- Barnett, Rachel E.;
- Matloff, Ellen T.
Publication type:
Article
Talking with Children About Adult-Onset Hereditary Cancer Risk: A Developmental Approach for Parents.
Published in:
Journal of Genetic Counseling, 2018, v. 27, n. 3, p. 533, doi. 10.1007/s10897-017-0191-7
By:
- Werner-Lin, Allison;
- Merrill, Shana L.;
- Brandt, Amanda C.
Publication type:
Article
Defects of mutant DNMT1 are linked to a spectrum of neurological disorders.
Published in:
Brain: A Journal of Neurology, 2015, v. 138, n. 4, p. 845, doi. 10.1093/brain/awv010
By:
- Baets, Jonathan;
- Xiaohui Duan;
- Yanhong Wu;
- Smith, Gordon;
- Seeley, William W.;
- Mademan, Inès;
- McGrath, Nicole M.;
- Beadell, Noah C.;
- Khoury, Julie;
- Botuyan, Maria-Victoria;
- Mer, Georges;
- Worrell, Gregory A.;
- Hojo, Kaori;
- DeLeon, Jessica;
- Laura, Matilde;
- Yo-Tsen Liu;
- Senderek, Jan;
- Weis, Joachim;
- Van den Bergh, Peter;
- Merrill, Shana L.
Publication type:
Article
Inherited Mutations in Pheochromocytoma and Paraganglioma: Why All Patients Should Be Offered Genetic Testing.
Published in:
Annals of Surgical Oncology: An Oncology Journal for Surgeons, 2013, v. 20, n. 5, p. 1444, doi. 10.1245/s10434-013-2942-5
By:
- Fishbein, Lauren;
- Merrill, Shana;
- Fraker, Douglas;
- Cohen, Debbie;
- Nathanson, Katherine
Publication type:
Article
Gain of Function for the <italic>SCN1A</italic>/hNa<sub>v</sub>1.1-L1670W Mutation Responsible for Familial Hemiplegic Migraine.
Published in:
Frontiers in Molecular Neuroscience, 2018, p. N.PAG, doi. 10.3389/fnmol.2018.00232
By:
- Dhifallah, Sandra;
- Lancaster, Eric;
- Merrill, Shana;
- Leroudier, Nathalie;
- Mantegazza, Massimo;
- Cestèle, Sandrine
Publication type:
Article
Whole-exome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas.
Published in:
Nature Communications, 2015, v. 6, n. 1, p. 6140, doi. 10.1038/ncomms7140
By:
- Fishbein, Lauren;
- Khare, Sanika;
- Wubbenhorst, Bradley;
- DeSloover, Daniel;
- D'Andrea, Kurt;
- Merrill, Shana;
- Cho, Nam Woo;
- Greenberg, Roger A.;
- Else, Tobias;
- Montone, Kathleen;
- LiVolsi, Virginia;
- Fraker, Douglas;
- Daber, Robert;
- Cohen, Debbie L.;
- Nathanson, Katherine L.
Publication type:
Article
Fanconi anemia caused by biallelic inactivation of BRCA2 can present with an atypical cancer phenotype in adulthood.
Published in:
Clinical Genetics, 2023, v. 103, n. 1, p. 119, doi. 10.1111/cge.14231
By:
- Maxwell, Kara N.;
- Patel, Vishal;
- Nead, Kevin T.;
- Merrill, Shana;
- Clark, Dana;
- Jiang, Qinqin;
- Wubbenhorst, Bradley;
- D'Andrea, Kurt;
- Cohen, Roger B.;
- Domchek, Susan M.;
- Morrissette, Jennifer J. D.;
- Greenberg, Roger A.;
- Babushok, Daria V.;
- Nathanson, Katherine L.
Publication type:
Article
Waiting and "weighted down": the challenge of anticipatory loss for individuals and families with Li-Fraumeni Syndrome.
Published in:
Familial Cancer, 2020, v. 19, n. 3, p. 259, doi. 10.1007/s10689-020-00173-6
By:
- Werner-Lin, Allison;
- Young, Jennifer L.;
- Wilsnack, Catherine;
- Merrill, Shana L.;
- Groner, Victoria;
- Greene, Mark H.;
- Khincha, Payal P.
Publication type:
Article
Family Identity and Roles in the Context of Li-Fraumeni Syndrome: "No One's Like Us Mutants".
Published in:
Health & Social Work, 2021, v. 46, n. 4, p. 299, doi. 10.1093/hsw/hlab032
By:
- Wilsnack, Catherine;
- Young, Jennifer L.;
- Merrill, Shana L.;
- Groner, Victoria;
- Loud, Jennifer T.;
- Bremer, Renee C.;
- Greene, Mark H.;
- Khincha, Payal P.;
- Werner-Lin, Allison
Publication type:
Article

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