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Molecular basis of hexosamininidase a deficiency and pseudodeficiency in the Berks County Pennsylvania Dutch.
Published in:
Human Mutation, 1992, v. 1, n. 4, p. 298, doi. 10.1002/humu.1380010406
By:
- Mules, Emilie H.;
- Hayflick, Susan;
- Dowling, Carol E.;
- Kelly, Thaddeus E.;
- Akerman, Beverly R.;
- Gravel, Roy A.;
- Thomas, George H.
Publication type:
Article
Dramatically Different Phenotypes in Mouse Models of Human Tay-Sachs and Sandhoff Diseases.
Published in:
Human Molecular Genetics, 1996, v. 5, n. 1, p. 1, doi. 10.1093/hmg/5.1.1
By:
- Phaneuf, Daniel;
- Wakamatsu, Nobuaki;
- Huang, Jing-Qi;
- Borowski, Anita;
- Peterson, Alan C.;
- Fortunato, Sheila R.;
- Ritter, Gerd;
- Igdoura, Suleiman A.;
- Morales, Carlos R.;
- Benoit, Guylaine;
- Akerman, Beverly R.;
- Leclerc, Daniel;
- Hanai, Nobuo;
- Marth, Jamey D.;
- Trasler, Jacquetta M.;
- Gravel, Roy A.
Publication type:
Article
A second, large deletion in the HEXB gene in a patient with infantile Sandhoff disease.
Published in:
Human Molecular Genetics, 1995, v. 4, n. 4, p. 777
By:
- Zhang, Zhi-Xin;
- Wakamatsu, Nobuaki;
- Akerman, Beverly R.;
- Mules, Emily H.;
- Thomas, George H.;
- Gravel, Roy A.
Publication type:
Article
Reflections on the birth of conjoined twins.
Published in:
2007
By:
- Akerman, Beverly R
Publication type:
commentary