Tama Sobe : rechercher sur Z-Library

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1

Genetics of congenital deafness in the Palestinian population: multiple connexin

Hashem Shahin, Tom Walsh, Tama Sobe, Eric Lynch, Mary-Claire King, Karen B. Avraham, Moien Kanaan

Journal:

Année:

2002

Langue:

english

Fichier:

PDF, 155 KB

english, 2002

2

High frequency of the deafness-associated 167delT mutation in the connexin 26 (GJB2) gene in Israeli Ashkenazim

Sobe, Tama, Erlich, Porat, Berry, Asher, Korostichevsky, Michael, Vreugde, Sarah, Avraham, Karen B., Bonn�-Tamir, Batsheva, Shohat, Mordechai

Journal:

American Journal of Medical Genetics

Année:

1999

Langue:

english

Fichier:

PDF, 40 KB

english, 1999

3

Clinical, Cellular, and Molecular Features of an Israeli Xeroderma Pigmentosum Family with a Frameshift Mutation in the XPC Gene: Sun Protection Prolongs Life

Slor, Hanoch, Batko, Sima, Khan, Sikandar G, Sobe, Tama, Emmert, Steffen, Khadavi, Arash, Frumkin, Azriel, Busch, David B, Albert, Roberta B, Kraemer, Kenneth H

Journal:

The Journal of Investigative Dermatology

Année:

2000

Langue:

english

Fichier:

PDF, 249 KB

english, 2000

4

Role of Myosin VI in the Differentiation of Cochlear Hair Cells

Tim Self, Tama Sobe, Neal G. Copeland, Nancy A. Jenkins, Karen B. Avraham, Karen P. Steel

Journal:

Developmental Biology

Année:

1999

Langue:

english

Fichier:

PDF, 1.10 MB

english, 1999

5

Genomic structure of the human unconventional myosin VI gene

Nadav Ahituv, Tama Sobe, Nahid G Robertson, Cynthia C Morton, R.Thomas Taggart, Karen B Avraham

Journal:

Année:

2000

Langue:

english

Fichier:

PDF, 115 KB

english, 2000

6

MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss

Salvatore Melchionda, Nadav Ahituv, Luigi Bisceglia, Tama Sobe, Fabian Glaser, Raquel Rabionet, Maria Lourdes Arbones, Angelo Notarangelo, Enzo Di Iorio, Massimo Carella, Leopoldo Zelante, Xavier Esti

Journal:

The American Journal of Human Genetics

Année:

2001

Langue:

english

Fichier:

PDF, 844 KB

english, 2001

7

Mutations in a Novel Isoform of TRIOBP That Encodes a Filamentous-Actin Binding Protein Are Responsible for DFNB28 Recessive Nonsyndromic Hearing Loss

Hashem Shahin, Tom Walsh, Tama Sobe, Judeh Abu Sa’ed, Amal Abu Rayan, Eric D. Lynch, Ming K. Lee, Karen B. Avraham, Mary-Claire King, Moein Kanaan

Journal:

The American Journal of Human Genetics

Année:

2006

Langue:

english

Fichier:

PDF, 2.37 MB

english, 2006