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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 analysis
X Bu, M Shohat, L Jaber, et al.
Clinical Genetics
|
October 1, 1995
Late diagnosis of Down syndrome due to incorrect cytogenetic diagnosis and extreme prematurity
M Druce, I J Cohen, N Naor, et al.
American Journal of Medical Genetics
|
June 27, 1997
Consanguinity and common adult diseases in Israeli Arab communities
L Jaber, T Shohat, J I Rotter, et al.
Pediatrics
|
January 1, 1984
Neonatal polycythemia: II. Definition related to time of sampling
M Shohat, S H Reisner, F Mimouni, et al.
Archives of Disease in Childhood
|
September 1, 1996
Familial hypothyroidism with autosomal dominant inheritance
M Mimouni, A Mimouni-Bloch, J Schachter, et al.
Israel Journal of Medical Sciences
|
April 1, 1988
Cerebrospinal fluid findings in infants with nonpolio enteroviral meningitis
M Shohat, T Lerman-Sagie, Y Levy, et al.
Clinical Genetics
|
July 18, 2002
Facial clefting in an Arab town in Israel
L 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 retardation
Y 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 Israel
M Daniels, T Shohat, A Brenner-Ullman, et al.
Page
of 19
Search research articles
Search
Showing results (61-70 of 190) with videos related to
Sort By:
Page
of 19
Genetic Epidemiology
|
January 1, 1993
A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis
X Bu, M Shohat, L Jaber, et al.
Clinical Genetics
|
October 1, 1995
Late diagnosis of Down syndrome due to incorrect cytogenetic diagnosis and extreme prematurity
M Druce, I J Cohen, N Naor, et al.
American Journal of Medical Genetics
|
June 27, 1997
Consanguinity and common adult diseases in Israeli Arab communities
L Jaber, T Shohat, J I Rotter, et al.
Pediatrics
|
January 1, 1984
Neonatal polycythemia: II. Definition related to time of sampling
M Shohat, S H Reisner, F Mimouni, et al.
Archives of Disease in Childhood
|
September 1, 1996
Familial hypothyroidism with autosomal dominant inheritance
M Mimouni, A Mimouni-Bloch, J Schachter, et al.
Israel Journal of Medical Sciences
|
April 1, 1988
Cerebrospinal fluid findings in infants with nonpolio enteroviral meningitis
M Shohat, T Lerman-Sagie, Y Levy, et al.
Clinical Genetics
|
July 18, 2002
Facial clefting in an Arab town in Israel
L 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 retardation
Y 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 Israel
M Daniels, T Shohat, A Brenner-Ullman, et al.
Page
of 19