Identification of novel mutations in Pakistani families with autosomal recessive retinitis pigmentosa. 2011

Maleeha Azam, and Rob W J Collin, and Ayesha Malik, and Muhammad I Khan, and Syed Tahir A Shah, and Aftab A Shah, and Alamdar Hussain, and Ahmed Sadeque, and Kentar Arimadyo, and Muhammad Ajmal, and Ayesha Azam, and Nadeem Qureshi, and Habib Bokhari, and Tim M Strom, and Frans P M Cremers, and Raheel Qamar, and Anneke I den Hollander

UI MeSH Term Description Entries
D008040 Genetic Linkage The co-inheritance of two or more non-allelic GENES due to their being located more or less closely on the same CHROMOSOME. Genetic Linkage Analysis,Linkage, Genetic,Analyses, Genetic Linkage,Analysis, Genetic Linkage,Genetic Linkage Analyses,Linkage Analyses, Genetic,Linkage Analysis, Genetic
D009154 Mutation Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations. Mutations
D010154 Pakistan A country located in southern Asia, bordering the Arabian Sea, between India on the east and Iran and Afghanistan on the west and China in the north. The capital is Islamabad. Islamic Republic of Pakistan
D003241 Consanguinity The magnitude of INBREEDING in humans. Inbreeding, Human,Consanguineous Marriage,Consanguinous Mating,Consanguineous Marriages,Consanguinities,Consanguinous Matings,Human Inbreeding,Human Inbreedings,Inbreedings, Human,Marriage, Consanguineous,Marriages, Consanguineous,Mating, Consanguinous,Matings, Consanguinous
D004252 DNA Mutational Analysis Biochemical identification of mutational changes in a nucleotide sequence. Mutational Analysis, DNA,Analysis, DNA Mutational,Analyses, DNA Mutational,DNA Mutational Analyses,Mutational Analyses, DNA
D005808 Genes, Recessive Genes that influence the PHENOTYPE only in the homozygous state. Conditions, Recessive Genetic,Genetic Conditions, Recessive,Recessive Genetic Conditions,Condition, Recessive Genetic,Gene, Recessive,Genetic Condition, Recessive,Recessive Gene,Recessive Genes,Recessive Genetic Condition
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D012174 Retinitis Pigmentosa Hereditary, progressive degeneration of the retina due to death of ROD PHOTORECEPTORS initially and subsequent death of CONE PHOTORECEPTORS. It is characterized by deposition of pigment in the retina. Pigmentary Retinopathy,Tapetoretinal Degeneration,Pigmentary Retinopathies,Retinopathies, Pigmentary,Retinopathy, Pigmentary,Tapetoretinal Degenerations
D055106 Genome-Wide Association Study An analysis comparing the allele frequencies of all available (or a whole GENOME representative set of) polymorphic markers to identify gene candidates or quantitative trait loci associated with a specific organism trait or specific disease or condition. Genome Wide Association Analysis,Genome Wide Association Study,GWA Study,Genome Wide Association Scan,Genome Wide Association Studies,Whole Genome Association Analysis,Whole Genome Association Study,Association Studies, Genome-Wide,Association Study, Genome-Wide,GWA Studies,Genome-Wide Association Studies,Studies, GWA,Studies, Genome-Wide Association,Study, GWA,Study, Genome-Wide Association
D018895 Microsatellite Repeats A variety of simple repeat sequences that are distributed throughout the GENOME. They are characterized by a short repeat unit of 2-8 basepairs that is repeated up to 100 times. They are also known as short tandem repeats (STRs). Microsatellite Markers,Pentanucleotide Repeats,Simple Repetitive Sequence,Tetranucleotide Repeats,Microsatellites,Short Tandem Repeats,Simple Sequence Repeats,Marker, Microsatellite,Markers, Microsatellite,Microsatellite,Microsatellite Marker,Microsatellite Repeat,Pentanucleotide Repeat,Repeat, Microsatellite,Repeat, Pentanucleotide,Repeat, Short Tandem,Repeat, Simple Sequence,Repeat, Tetranucleotide,Repeats, Microsatellite,Repeats, Pentanucleotide,Repeats, Short Tandem,Repeats, Simple Sequence,Repeats, Tetranucleotide,Repetitive Sequence, Simple,Repetitive Sequences, Simple,Sequence Repeat, Simple,Sequence Repeats, Simple,Sequence, Simple Repetitive,Sequences, Simple Repetitive,Short Tandem Repeat,Simple Repetitive Sequences,Simple Sequence Repeat,Tandem Repeat, Short,Tandem Repeats, Short,Tetranucleotide Repeat

Related Publications

Maleeha Azam, and Rob W J Collin, and Ayesha Malik, and Muhammad I Khan, and Syed Tahir A Shah, and Aftab A Shah, and Alamdar Hussain, and Ahmed Sadeque, and Kentar Arimadyo, and Muhammad Ajmal, and Ayesha Azam, and Nadeem Qureshi, and Habib Bokhari, and Tim M Strom, and Frans P M Cremers, and Raheel Qamar, and Anneke I den Hollander
July 2005, Investigative ophthalmology & visual science,
Maleeha Azam, and Rob W J Collin, and Ayesha Malik, and Muhammad I Khan, and Syed Tahir A Shah, and Aftab A Shah, and Alamdar Hussain, and Ahmed Sadeque, and Kentar Arimadyo, and Muhammad Ajmal, and Ayesha Azam, and Nadeem Qureshi, and Habib Bokhari, and Tim M Strom, and Frans P M Cremers, and Raheel Qamar, and Anneke I den Hollander
January 2013, Molecular vision,
Maleeha Azam, and Rob W J Collin, and Ayesha Malik, and Muhammad I Khan, and Syed Tahir A Shah, and Aftab A Shah, and Alamdar Hussain, and Ahmed Sadeque, and Kentar Arimadyo, and Muhammad Ajmal, and Ayesha Azam, and Nadeem Qureshi, and Habib Bokhari, and Tim M Strom, and Frans P M Cremers, and Raheel Qamar, and Anneke I den Hollander
January 2011, Molecular vision,
Maleeha Azam, and Rob W J Collin, and Ayesha Malik, and Muhammad I Khan, and Syed Tahir A Shah, and Aftab A Shah, and Alamdar Hussain, and Ahmed Sadeque, and Kentar Arimadyo, and Muhammad Ajmal, and Ayesha Azam, and Nadeem Qureshi, and Habib Bokhari, and Tim M Strom, and Frans P M Cremers, and Raheel Qamar, and Anneke I den Hollander
September 2019, Molecular medicine reports,
Maleeha Azam, and Rob W J Collin, and Ayesha Malik, and Muhammad I Khan, and Syed Tahir A Shah, and Aftab A Shah, and Alamdar Hussain, and Ahmed Sadeque, and Kentar Arimadyo, and Muhammad Ajmal, and Ayesha Azam, and Nadeem Qureshi, and Habib Bokhari, and Tim M Strom, and Frans P M Cremers, and Raheel Qamar, and Anneke I den Hollander
September 2022, Iranian journal of public health,
Maleeha Azam, and Rob W J Collin, and Ayesha Malik, and Muhammad I Khan, and Syed Tahir A Shah, and Aftab A Shah, and Alamdar Hussain, and Ahmed Sadeque, and Kentar Arimadyo, and Muhammad Ajmal, and Ayesha Azam, and Nadeem Qureshi, and Habib Bokhari, and Tim M Strom, and Frans P M Cremers, and Raheel Qamar, and Anneke I den Hollander
May 2005, Journal of medical genetics,
Maleeha Azam, and Rob W J Collin, and Ayesha Malik, and Muhammad I Khan, and Syed Tahir A Shah, and Aftab A Shah, and Alamdar Hussain, and Ahmed Sadeque, and Kentar Arimadyo, and Muhammad Ajmal, and Ayesha Azam, and Nadeem Qureshi, and Habib Bokhari, and Tim M Strom, and Frans P M Cremers, and Raheel Qamar, and Anneke I den Hollander
November 2004, Molecular vision,
Maleeha Azam, and Rob W J Collin, and Ayesha Malik, and Muhammad I Khan, and Syed Tahir A Shah, and Aftab A Shah, and Alamdar Hussain, and Ahmed Sadeque, and Kentar Arimadyo, and Muhammad Ajmal, and Ayesha Azam, and Nadeem Qureshi, and Habib Bokhari, and Tim M Strom, and Frans P M Cremers, and Raheel Qamar, and Anneke I den Hollander
March 2021, JPMA. The Journal of the Pakistan Medical Association,
Maleeha Azam, and Rob W J Collin, and Ayesha Malik, and Muhammad I Khan, and Syed Tahir A Shah, and Aftab A Shah, and Alamdar Hussain, and Ahmed Sadeque, and Kentar Arimadyo, and Muhammad Ajmal, and Ayesha Azam, and Nadeem Qureshi, and Habib Bokhari, and Tim M Strom, and Frans P M Cremers, and Raheel Qamar, and Anneke I den Hollander
March 2015, Scientific reports,
Maleeha Azam, and Rob W J Collin, and Ayesha Malik, and Muhammad I Khan, and Syed Tahir A Shah, and Aftab A Shah, and Alamdar Hussain, and Ahmed Sadeque, and Kentar Arimadyo, and Muhammad Ajmal, and Ayesha Azam, and Nadeem Qureshi, and Habib Bokhari, and Tim M Strom, and Frans P M Cremers, and Raheel Qamar, and Anneke I den Hollander
May 2007, Annals of human genetics,
Copied contents to your clipboard!