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Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko
|
July 1, 1980
[Agenesis of the corpus callosum]
V G Antonenko, O P Robak
Genetika
|
December 1, 1985
[A new case of trisomy 5p]
V G Antonenko, L Ia Levina, V I Chudnova
Pediatriia
|
January 1, 1991
[Approach to differential diagnosis of clinically related forms of chromosomal pathology using computers]
V G Antonenko, L Ia Levina, L M Konstantinova, et al.
Klinicheskaia Khirurgiia
|
January 1, 1989
[Results of stereotaxic operations in patients with neurosurgical pathology]
O A Laponogov, V I Tsymbaliuk, N G Matiuk, et al.
Vestnik Rossiiskoi Akademii Meditsinskikh Nauk
|
July 6, 2000
[Study of CATCH 22: genetic aspects]
V G Antonenko, V I Ivanov, L M Konstantinova, et al.
Vestnik Rossiiskoi Akademii Meditsinskikh Nauk
|
January 1, 1992
[Computerized analysis in the study of multiple congenital defects connected with chromosome abnormalities: phenotype-karyotypic relations and genetic markers]
V I Ivanov, L Ia Levina, L M Konstantinova, et al.
Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko
|
January 1, 1990
[Our experience with 2220 stereotaxic operations]
O A Laponogov, V I Tsymbaliuk, N G Matiuk, et al.
Genetika
|
December 6, 2014
[Generation and application of dynamic standard reference intervals for analyzing results of comparative genomic hybridization]
M E Min'zhenkova, N V Shilova, Zh G Markova, et al.
American Journal of Medical Genetics. Part A
|
November 18, 2008
Unique mosaic X/Y translocation/insertion in infant 45,X male
V B Chernykh, S V Vyatkina, V G Antonenko, et al.
Genetika
|
February 27, 2015
[Genetic and clinical characteristics of 22q11.2 deletion syndrome]
Iu O Kozlova, V V Zabnenkova, N V Shilova, et al.
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Showing results (1-10 of 10) with videos related to
Sort By:
Page
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Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko
|
July 1, 1980
[Agenesis of the corpus callosum]
V G Antonenko, O P Robak
Genetika
|
December 1, 1985
[A new case of trisomy 5p]
V G Antonenko, L Ia Levina, V I Chudnova
Pediatriia
|
January 1, 1991
[Approach to differential diagnosis of clinically related forms of chromosomal pathology using computers]
V G Antonenko, L Ia Levina, L M Konstantinova, et al.
Klinicheskaia Khirurgiia
|
January 1, 1989
[Results of stereotaxic operations in patients with neurosurgical pathology]
O A Laponogov, V I Tsymbaliuk, N G Matiuk, et al.
Vestnik Rossiiskoi Akademii Meditsinskikh Nauk
|
July 6, 2000
[Study of CATCH 22: genetic aspects]
V G Antonenko, V I Ivanov, L M Konstantinova, et al.
Vestnik Rossiiskoi Akademii Meditsinskikh Nauk
|
January 1, 1992
[Computerized analysis in the study of multiple congenital defects connected with chromosome abnormalities: phenotype-karyotypic relations and genetic markers]
V I Ivanov, L Ia Levina, L M Konstantinova, et al.
Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko
|
January 1, 1990
[Our experience with 2220 stereotaxic operations]
O A Laponogov, V I Tsymbaliuk, N G Matiuk, et al.
Genetika
|
December 6, 2014
[Generation and application of dynamic standard reference intervals for analyzing results of comparative genomic hybridization]
M E Min'zhenkova, N V Shilova, Zh G Markova, et al.
American Journal of Medical Genetics. Part A
|
November 18, 2008
Unique mosaic X/Y translocation/insertion in infant 45,X male
V B Chernykh, S V Vyatkina, V G Antonenko, et al.
Genetika
|
February 27, 2015
[Genetic and clinical characteristics of 22q11.2 deletion syndrome]
Iu O Kozlova, V V Zabnenkova, N V Shilova, et al.
Page
of 1