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American Journal of Medical Genetics
|
July 27, 2001
Comments on biological asymmetry
J M Opitz, A Utkus
Balkan Journal of Medical Genetics : BJMG
|
March 15, 2017
A novel intronic splice site <i>tafazzin</i> gene mutation detected prenatally in a family with Barth syndrome
M Bakšienė, E Benušienė, A Morkūnienė, et al.
Journal of Applied Genetics
|
September 22, 2017
Phenotype comparison confirms ZMYND11 as a critical gene for 10p15.3 microdeletion syndrome
Birute Tumiene, Ž Čiuladaitė, E Preikšaitienė, et al.
American Journal of Medical Genetics
|
June 8, 2001
Human anotocephaly (aprosopus, acrania-synotia) in the Vilnius anatomical collection
A Utkus, R Kazakevicius, R Ptasekas, et al.
Balkan Journal of Medical Genetics : BJMG
|
November 15, 2018
Acute Pre-B Lymphoblastic Leukemia and Congenital Anomalies in a Child with a <i>de Novo</i> 22q11.1q11.22 Duplication
M Vaisvilas, V Dirse, B Aleksiuniene, et al.
Cytogenetic and Genome Research
|
October 6, 2012
Two new de novo interstitial duplications covering 2p14-p22.1: clinical and molecular analysis
J Kasnauskiene, L Cimbalistiene, A Utkus, et al.
Journal of Medical Genetics
|
February 9, 1999
Duplication of segment 1p21 following paternal insertional translocation, ins(6;1)(q25;p13.3p22.1)
A Utkus, I Sorokina, V Kucinskas, et al.
European Journal of Medical Genetics
|
July 31, 2012
A novel de novo 1.8 Mb microdeletion of 17q21.33 associated with intellectual disability and dysmorphic features
E Preiksaitiene, K Männik, V Dirse, et al.
Clinical Genetics
|
September 13, 2006
Hereditary lymphedema type I associated with VEGFR3 mutation: the first de novo case and atypical presentations
A Ghalamkarpour, S Morlot, A Raas-Rothschild, et al.
Genetic Testing
|
October 6, 2006
Molecular basis of cystic fibrosis in Lithuania: incomplete CFTR mutation detection by PCR-based screening protocols
S Giannattasio, A Bobba, V Jurgelevicius, et al.
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Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
American Journal of Medical Genetics
|
July 27, 2001
Comments on biological asymmetry
J M Opitz, A Utkus
Balkan Journal of Medical Genetics : BJMG
|
March 15, 2017
A novel intronic splice site <i>tafazzin</i> gene mutation detected prenatally in a family with Barth syndrome
M Bakšienė, E Benušienė, A Morkūnienė, et al.
Journal of Applied Genetics
|
September 22, 2017
Phenotype comparison confirms ZMYND11 as a critical gene for 10p15.3 microdeletion syndrome
Birute Tumiene, Ž Čiuladaitė, E Preikšaitienė, et al.
American Journal of Medical Genetics
|
June 8, 2001
Human anotocephaly (aprosopus, acrania-synotia) in the Vilnius anatomical collection
A Utkus, R Kazakevicius, R Ptasekas, et al.
Balkan Journal of Medical Genetics : BJMG
|
November 15, 2018
Acute Pre-B Lymphoblastic Leukemia and Congenital Anomalies in a Child with a <i>de Novo</i> 22q11.1q11.22 Duplication
M Vaisvilas, V Dirse, B Aleksiuniene, et al.
Cytogenetic and Genome Research
|
October 6, 2012
Two new de novo interstitial duplications covering 2p14-p22.1: clinical and molecular analysis
J Kasnauskiene, L Cimbalistiene, A Utkus, et al.
Journal of Medical Genetics
|
February 9, 1999
Duplication of segment 1p21 following paternal insertional translocation, ins(6;1)(q25;p13.3p22.1)
A Utkus, I Sorokina, V Kucinskas, et al.
European Journal of Medical Genetics
|
July 31, 2012
A novel de novo 1.8 Mb microdeletion of 17q21.33 associated with intellectual disability and dysmorphic features
E Preiksaitiene, K Männik, V Dirse, et al.
Clinical Genetics
|
September 13, 2006
Hereditary lymphedema type I associated with VEGFR3 mutation: the first de novo case and atypical presentations
A Ghalamkarpour, S Morlot, A Raas-Rothschild, et al.
Genetic Testing
|
October 6, 2006
Molecular basis of cystic fibrosis in Lithuania: incomplete CFTR mutation detection by PCR-based screening protocols
S Giannattasio, A Bobba, V Jurgelevicius, et al.
Page
of 2