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Page 1
Genomics of rare genetic diseases-experiences from India.
Hum Genomics. 2019 Sep 25;14(1):52. doi: 10.1186/s40246-019-0215-5.
Hum Genomics. 2019.
PMID: 31554517
Free PMC article.
Review.
Prevalence of β-thalassemia and other haemoglobinopathies in six cities in India: a multicentre study.
Mohanty D, Colah RB, Gorakshakar AC, Patel RZ, Master DC, Mahanta J, Sharma SK, Chaudhari U, Ghosh M, Das S, Britt RP, Singh S, Ross C, Jagannathan L, Kaul R, Shukla DK, Muthuswamy V.
Mohanty D, et al. Among authors: master dc.
J Community Genet. 2013 Jan;4(1):33-42. doi: 10.1007/s12687-012-0114-0. Epub 2012 Oct 21.
J Community Genet. 2013.
PMID: 23086467
Free PMC article.
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Hidradenitis suppurativa (or Acne inversa) with autosomal dominant inheritance is not linked to chromosome 1p21.1-1q25.3 region.
Al-Ali FM, Ratnamala U, Mehta TY, Naveed M, Al-Ali MT, Al-Khaja N, Sheth JJ, Master DC, Maiti AK, Chetan GK, Nath SK, Radhakrishna U.
Al-Ali FM, et al. Among authors: master dc.
Exp Dermatol. 2010 Sep;19(9):851-3. doi: 10.1111/j.1600-0625.2010.01088.x.
Exp Dermatol. 2010.
PMID: 20698881
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China's forest policy for the 21st century.
Zhang P, Shao G, Zhao G, Le Master DC, Parker GR, Dunning JB Jr, Li Q.
Zhang P, et al. Among authors: le master dc.
Science. 2000 Jun 23;288(5474):2135-6. doi: 10.1126/science.288.5474.2135.
Science. 2000.
PMID: 10896587
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Exome sequencing reveals a novel mutation, p.L325H, in the KRT5 gene associated with autosomal dominant Epidermolysis Bullosa Simplex Koebner type in a large family from western India.
Vellarikkal SK, Patowary A, Singh M, Kumari R, Faruq M, Master DC, Sivasubbu S, Scaria V.
Vellarikkal SK, et al. Among authors: master dc.
Hum Genome Var. 2014 Sep 4;1:14007. doi: 10.1038/hgv.2014.7. eCollection 2014.
Hum Genome Var. 2014.
PMID: 27081501
Free PMC article.
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Interaction of iron deficiency anemia and hemoglobinopathies among college students and pregnant women: a multi center evaluation in India.
Mohanty D, Gorakshakar AC, Colah RB, Patel RZ, Master DC, Mahanta J, Sharma SK, Chaudhari U, Ghosh M, Das S, Britt RP, Singh S, Ross C, Jagannathan L, Kaul R, Shukla DK, Muthuswamy V.
Mohanty D, et al. Among authors: master dc.
Hemoglobin. 2014;38(4):252-7. doi: 10.3109/03630269.2014.913517.
Hemoglobin. 2014.
PMID: 25023086
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Genomewide scan for nonsyndromic cleft lip and palate in multigenerational Indian families reveals significant evidence of linkage at 13q33.1-34.
Radhakrishna U, Ratnamala U, Gaines M, Beiraghi S, Hutchings D, Golla J, Husain SA, Gambhir PS, Sheth JJ, Sheth FJ, Chetan GK, Naveed M, Solanki JV, Patel UC, Master DC, Memon R, Antonarakis GS, Antonarakis SE, Nath SK.
Radhakrishna U, et al. Among authors: master dc.
Am J Hum Genet. 2006 Sep;79(3):580-5. doi: 10.1086/507487. Epub 2006 Jul 21.
Am J Hum Genet. 2006.
PMID: 16909398
Free PMC article.
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