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Journal of Medical Genetics
|
October 1, 1987
A family with spondyloepimetaphyseal dwarfism: a 'new' dysplasia or Kniest disease with autosomal recessive inheritance?
T I Farag, S A Al-Awadi, M C Hunt, et al.
Indian Dermatology Online Journal
|
May 7, 2021
Assessment of Patients with Periorbital Melanosis for Hyperinsulinemia and Insulin Resistance
Devinder M Thappa, Laxmisha Chandrashekar, Medha Rajappa, et al.
European Journal of Medical Genetics
|
May 17, 2021
Utility of clinical exome sequencing in the evaluation of neonates with suspected genetic condition - An observational study from tertiary neonatal care unit in South India
R Usha Devi, J Thinesh Kumar, Shaik Mohammad Shafi Jan, et al.
American Journal of Medical Genetics
|
March 17, 1997
Kenny-Caffey syndrome in six Bedouin sibships: autosomal recessive inheritance is confirmed
K Tahseen, S Khan, R Uma, et al.
Virology
|
November 1, 1993
Expression of an animal virus antigenic site on the surface of a plant virus particle
R Usha, J B Rohll, V E Spall, et al.
Virus Genes
|
March 12, 2013
First report of an alphasatellite associated with Okra enation leaf curl virus
S A Chandran, R M Packialakshmi, K Subhalakshmi, et al.
American Journal of Medical Genetics
|
April 1, 1986
Interstitial deletion of the long arm of chromosome 1 [del(1)(q32q42)]
S A Al-Awadi, T I Farag, R Usha, et al.
Experimental Cell Research
|
November 14, 2017
Human papillomavirus (HPV) oncoprotein E6 facilitates Calcineurin-Nuclear factor for activated T cells 2 (NFAT2) signaling to promote cellular proliferation in cervical cell carcinoma
Babul Moni Ram, Jayashree Dolpady, Rakesh Kulkarni, et al.
Neurochemical Research
|
March 22, 2014
Potential contribution of monoamine oxidase a gene variants in ADHD and behavioral co-morbidities: scenario in eastern Indian probands
A Karmakar, S Maitra, D Verma, et al.
American Journal of Medical Genetics
|
December 1, 1992
Late diagnosis of phenylketonuria in a Bedouin mother
R Usha, R Uma, T I Farag, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 105) with videos related to
Sort By:
Page
of 11
Journal of Medical Genetics
|
October 1, 1987
A family with spondyloepimetaphyseal dwarfism: a 'new' dysplasia or Kniest disease with autosomal recessive inheritance?
T I Farag, S A Al-Awadi, M C Hunt, et al.
Indian Dermatology Online Journal
|
May 7, 2021
Assessment of Patients with Periorbital Melanosis for Hyperinsulinemia and Insulin Resistance
Devinder M Thappa, Laxmisha Chandrashekar, Medha Rajappa, et al.
European Journal of Medical Genetics
|
May 17, 2021
Utility of clinical exome sequencing in the evaluation of neonates with suspected genetic condition - An observational study from tertiary neonatal care unit in South India
R Usha Devi, J Thinesh Kumar, Shaik Mohammad Shafi Jan, et al.
American Journal of Medical Genetics
|
March 17, 1997
Kenny-Caffey syndrome in six Bedouin sibships: autosomal recessive inheritance is confirmed
K Tahseen, S Khan, R Uma, et al.
Virology
|
November 1, 1993
Expression of an animal virus antigenic site on the surface of a plant virus particle
R Usha, J B Rohll, V E Spall, et al.
Virus Genes
|
March 12, 2013
First report of an alphasatellite associated with Okra enation leaf curl virus
S A Chandran, R M Packialakshmi, K Subhalakshmi, et al.
American Journal of Medical Genetics
|
April 1, 1986
Interstitial deletion of the long arm of chromosome 1 [del(1)(q32q42)]
S A Al-Awadi, T I Farag, R Usha, et al.
Experimental Cell Research
|
November 14, 2017
Human papillomavirus (HPV) oncoprotein E6 facilitates Calcineurin-Nuclear factor for activated T cells 2 (NFAT2) signaling to promote cellular proliferation in cervical cell carcinoma
Babul Moni Ram, Jayashree Dolpady, Rakesh Kulkarni, et al.
Neurochemical Research
|
March 22, 2014
Potential contribution of monoamine oxidase a gene variants in ADHD and behavioral co-morbidities: scenario in eastern Indian probands
A Karmakar, S Maitra, D Verma, et al.
American Journal of Medical Genetics
|
December 1, 1992
Late diagnosis of phenylketonuria in a Bedouin mother
R Usha, R Uma, T I Farag, et al.
Page
of 11