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H Bar El

Showing results (1-10 of 9) with videos related to

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American Journal of Medical Genetics|January 16, 1995
New heritable fragile site with spontaneous expression at 1q41H Dar, H Bar-El, M Ziv, et al.
British Journal of Haematology|September 6, 2000
Detection of translocation (16;16) in acute myeloid leukaemia (AML) patients by fluorescence in situ hybridization (FISH) using 16 telomer's probesH Dar, M Ziv, H Bar-El, et al.
American Journal of Medical Genetics|January 1, 1988
Paracentric inversion of Xq and ovarian dysfunctionH Dar, J Tal, H Bar-el, et al.
American Journal of Medical Genetics|August 1, 1994
Deletion of the short arm of chromosome 10 (10p13): report of a patient and reviewM Shapira, Z Borochowitz, H Bar-El, et al.
Journal of Child Neurology|August 1, 1997
Deletion (4)(q33 --> qter): a case report and review of the literatureZ Borochowitz, S A Shalev, I Yehudai, et al.
American Journal of Medical Genetics|December 31, 1997
Inherited inverted duplication of X chromosome in a male: report of a patient and review of the literatureM Shapira, H Dar, H Bar-El, et al.
American Journal of Medical Genetics|April 24, 1996
Interstitial deletion (6)q13q15R Gershoni-Baruch, H Mandel, H Bar El, et al.
Human Reproduction (Oxford, England)|July 13, 1999
Testicular fine needle aspiration: the alternative method for sperm retrieval in non-obstructive azoospermiaA Lewin, B Reubinoff, A Porat-Katz, et al.
Fetal Diagnosis and Therapy|March 1, 1995
Very low maternal serum unconjugated estriol and prenatal diagnosis of steroid sulfatase deficiencyM David, N Israel, R Merksamer, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics|January 16, 1995
New heritable fragile site with spontaneous expression at 1q41H Dar, H Bar-El, M Ziv, et al.
British Journal of Haematology|September 6, 2000
Detection of translocation (16;16) in acute myeloid leukaemia (AML) patients by fluorescence in situ hybridization (FISH) using 16 telomer's probesH Dar, M Ziv, H Bar-El, et al.
American Journal of Medical Genetics|January 1, 1988
Paracentric inversion of Xq and ovarian dysfunctionH Dar, J Tal, H Bar-el, et al.
American Journal of Medical Genetics|August 1, 1994
Deletion of the short arm of chromosome 10 (10p13): report of a patient and reviewM Shapira, Z Borochowitz, H Bar-El, et al.
Journal of Child Neurology|August 1, 1997
Deletion (4)(q33 --> qter): a case report and review of the literatureZ Borochowitz, S A Shalev, I Yehudai, et al.
American Journal of Medical Genetics|December 31, 1997
Inherited inverted duplication of X chromosome in a male: report of a patient and review of the literatureM Shapira, H Dar, H Bar-El, et al.
American Journal of Medical Genetics|April 24, 1996
Interstitial deletion (6)q13q15R Gershoni-Baruch, H Mandel, H Bar El, et al.
Human Reproduction (Oxford, England)|July 13, 1999
Testicular fine needle aspiration: the alternative method for sperm retrieval in non-obstructive azoospermiaA Lewin, B Reubinoff, A Porat-Katz, et al.
Fetal Diagnosis and Therapy|March 1, 1995
Very low maternal serum unconjugated estriol and prenatal diagnosis of steroid sulfatase deficiencyM David, N Israel, R Merksamer, et al.
Pageof 1