Search research articles
Contact Us
Filters
Showing results (51-60 of 60) with videos related to
Page
of 6
Sort By:
You have reached the last page of results.
This site can display upto 60 results.
Archiwum Medycyny Sadowej I Kryminologii
|
March 24, 2005
Population studies for STR loci (D3S1358, D5S818, D7S820, D18S51 and FGA) in NWFP and Sindhi populations of Pakistan for forensic use
M Saqib Shahzad, S Yassir Abbas Bokhari, Abdul Qayyum Rao, et al.
Clinical Genetics
|
September 20, 2007
Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan
S-I Kitajiri, R McNamara, T Makishima, et al.
Journal of Zhejiang University. Science. B
|
March 15, 2006
Somatic embryogenesis in wild relatives of cotton (Gossypium Spp.)
Abdul Qayyum Rao, S Sarfraz Hussain, M Saqib Shahzad, et al.
Hemoglobin
|
January 17, 2002
A multi-center study in order to further define the molecular basis of beta-thalassemia in Thailand, Pakistan, Sri Lanka, Mauritius, Syria, and India, and to develop a simple molecular diagnostic strategy by amplification refractory mutation system-polymerase chain reaction
J M Old, S N Khan, I Verma, et al.
American Journal of Human Genetics
|
June 21, 2002
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness
L M Astuto, J M Bork, M D Weston, et al.
American Journal of Human Genetics
|
November 25, 2000
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23
J M Bork, L M Peters, S Riazuddin, et al.
Genomics
|
March 8, 2014
exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels
B Maranhao, P Biswas, J L Duncan, et al.
Clinical Genetics
|
September 16, 2016
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome
R Faridi, A U Rehman, R J Morell, et al.
Molecular Psychiatry
|
July 27, 2016
Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability
S Riazuddin, M Hussain, A Razzaq, et al.
Molecular Psychiatry
|
September 2, 2018
Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability
S Riazuddin, M Hussain, A Razzaq, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 60) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 60 results.
Archiwum Medycyny Sadowej I Kryminologii
|
March 24, 2005
Population studies for STR loci (D3S1358, D5S818, D7S820, D18S51 and FGA) in NWFP and Sindhi populations of Pakistan for forensic use
M Saqib Shahzad, S Yassir Abbas Bokhari, Abdul Qayyum Rao, et al.
Clinical Genetics
|
September 20, 2007
Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan
S-I Kitajiri, R McNamara, T Makishima, et al.
Journal of Zhejiang University. Science. B
|
March 15, 2006
Somatic embryogenesis in wild relatives of cotton (Gossypium Spp.)
Abdul Qayyum Rao, S Sarfraz Hussain, M Saqib Shahzad, et al.
Hemoglobin
|
January 17, 2002
A multi-center study in order to further define the molecular basis of beta-thalassemia in Thailand, Pakistan, Sri Lanka, Mauritius, Syria, and India, and to develop a simple molecular diagnostic strategy by amplification refractory mutation system-polymerase chain reaction
J M Old, S N Khan, I Verma, et al.
American Journal of Human Genetics
|
June 21, 2002
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness
L M Astuto, J M Bork, M D Weston, et al.
American Journal of Human Genetics
|
November 25, 2000
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23
J M Bork, L M Peters, S Riazuddin, et al.
Genomics
|
March 8, 2014
exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels
B Maranhao, P Biswas, J L Duncan, et al.
Clinical Genetics
|
September 16, 2016
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome
R Faridi, A U Rehman, R J Morell, et al.
Molecular Psychiatry
|
July 27, 2016
Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability
S Riazuddin, M Hussain, A Razzaq, et al.
Molecular Psychiatry
|
September 2, 2018
Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability
S Riazuddin, M Hussain, A Razzaq, et al.
Page
of 6