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M Shohat

Showing results (61-70 of 190) with videos related to

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Genetic Epidemiology|January 1, 1993
A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysisX Bu, M Shohat, L Jaber, et al.
Clinical Genetics|October 1, 1995
Late diagnosis of Down syndrome due to incorrect cytogenetic diagnosis and extreme prematurityM Druce, I J Cohen, N Naor, et al.
American Journal of Medical Genetics|June 27, 1997
Consanguinity and common adult diseases in Israeli Arab communitiesL Jaber, T Shohat, J I Rotter, et al.
Pediatrics|January 1, 1984
Neonatal polycythemia: II. Definition related to time of samplingM Shohat, S H Reisner, F Mimouni, et al.
Archives of Disease in Childhood|September 1, 1996
Familial hypothyroidism with autosomal dominant inheritanceM Mimouni, A Mimouni-Bloch, J Schachter, et al.
Israel Journal of Medical Sciences|April 1, 1988
Cerebrospinal fluid findings in infants with nonpolio enteroviral meningitisM Shohat, T Lerman-Sagie, Y Levy, et al.
Clinical Genetics|July 18, 2002
Facial clefting in an Arab town in IsraelL Jaber, A Nahmani, G J Halpern, et al.
American Journal of Medical Genetics|January 8, 1999
Tsukahara syndrome of radioulnar synostosis, short stature, microcephaly, scoliosis, and mental retardationY Udler, G J Halpern, M Shohat, et al.
Harefuah|May 2, 1982
[Transient neonatal pustulosis]M Shohat, P Merlob, A Metzker, et al.
American Journal of Medical Genetics|January 30, 1995
Familial Mediterranean fever: high gene frequency among the non-Ashkenazic and Ashkenazic Jewish populations in IsraelM Daniels, T Shohat, A Brenner-Ullman, et al.
Pageof 19

Showing results (61-70 of 190) with videos related to

Sort By:
Pageof 19
Genetic Epidemiology|January 1, 1993
A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysisX Bu, M Shohat, L Jaber, et al.
Clinical Genetics|October 1, 1995
Late diagnosis of Down syndrome due to incorrect cytogenetic diagnosis and extreme prematurityM Druce, I J Cohen, N Naor, et al.
American Journal of Medical Genetics|June 27, 1997
Consanguinity and common adult diseases in Israeli Arab communitiesL Jaber, T Shohat, J I Rotter, et al.
Pediatrics|January 1, 1984
Neonatal polycythemia: II. Definition related to time of samplingM Shohat, S H Reisner, F Mimouni, et al.
Archives of Disease in Childhood|September 1, 1996
Familial hypothyroidism with autosomal dominant inheritanceM Mimouni, A Mimouni-Bloch, J Schachter, et al.
Israel Journal of Medical Sciences|April 1, 1988
Cerebrospinal fluid findings in infants with nonpolio enteroviral meningitisM Shohat, T Lerman-Sagie, Y Levy, et al.
Clinical Genetics|July 18, 2002
Facial clefting in an Arab town in IsraelL Jaber, A Nahmani, G J Halpern, et al.
American Journal of Medical Genetics|January 8, 1999
Tsukahara syndrome of radioulnar synostosis, short stature, microcephaly, scoliosis, and mental retardationY Udler, G J Halpern, M Shohat, et al.
Harefuah|May 2, 1982
[Transient neonatal pustulosis]M Shohat, P Merlob, A Metzker, et al.
American Journal of Medical Genetics|January 30, 1995
Familial Mediterranean fever: high gene frequency among the non-Ashkenazic and Ashkenazic Jewish populations in IsraelM Daniels, T Shohat, A Brenner-Ullman, et al.
Pageof 19