muhammad ikram ullah (7 resultados)

Taschenbuch. Condición: Neu. Genetic Studies In Punjabi Families With Primary Microcephaly (MCPH) | Genetics of Primary Microcephaly | Muhammad Ikram Ullah (u. a.) | Taschenbuch | 92 S. | Englisch | 2013 | LAP LAMBERT Academic Publishing | EAN 9783659436062 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.

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Condición: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Afridi AnilaAnila Afrida completed her MPhil in Genetics from Hazara University, Pakistan in 2012.Currently the author doing PhD in Molecular Genetics of wheat from Hazara University, Mansehra, Pakistan.The genus Triticum include.

Condición: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Ikram Ullah MuhammadMuhammad Ikram Ullah, Senior Teaching and Research Fellow/Health Professional Educationalist, Department of Biochemistry, University of Health Sciences, Lahore, Pakistan. Research interest includes genetic studies.

Kartoniert / Broschiert. Condición: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Khan Ikram ullahIkram ullah khan is pharmacist by profession and lecturer at Faculty of Pharmaceutical Sciences Government College University Faisalabad Pakistan. He holds a PhD degree in Pharmaceutical Sciences from University of St.

Taschenbuch. Condición: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Primary microcephaly (MCPH) is neurological disorder. It exhibits genetic heterogeneity. The genes identified in MCPH are Microcephalin gene at MCPH1 locus, WDR62 at MCPH2, CDK5RAP2 gene at MCPH3 locus, CEP152 at MCPH4, ASPM at MCPH5 locus, CENPJ at MCPH6 locus and STIL/SIL at MCPH7 locus. The objective of this study was to identify families from Punjab and to perform homozygosity mapping and DNA sequencing for mutation detection. We reported c.3978G>A; p.W1326X mutation in ASPM gene of MCPH families from Punjab. This is the most prevalent gene investigated for mutations in Pakistan. The identification of common mutation in ASPM gene in families with primary microcephaly analyzed in this study from Punjab and several other families of an apparently different ethnic group (Pashtun) revealed most probable involvement of common ancestry for this variant in these MCPH families. Further data should be explored so that centres for genetic counseling could be established to guide the people for avoiding blood relation marraiges.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 92 pp. Englisch.

Taschenbuch. Condición: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Primary microcephaly (MCPH) is neurological disorder. It exhibits genetic heterogeneity. The genes identified in MCPH are Microcephalin gene at MCPH1 locus, WDR62 at MCPH2, CDK5RAP2 gene at MCPH3 locus, CEP152 at MCPH4, ASPM at MCPH5 locus, CENPJ at MCPH6 locus and STIL/SIL at MCPH7 locus. The objective of this study was to identify families from Punjab and to perform homozygosity mapping and DNA sequencing for mutation detection. We reported c.3978GA; p.W1326X mutation in ASPM gene of MCPH families from Punjab. This is the most prevalent gene investigated for mutations in Pakistan. The identification of common mutation in ASPM gene in families with primary microcephaly analyzed in this study from Punjab and several other families of an apparently different ethnic group (Pashtun) revealed most probable involvement of common ancestry for this variant in these MCPH families. Further data should be explored so that centres for genetic counseling could be established to guide the people for avoiding blood relation marraiges.