Utility of whole-exome sequencing in detecting novel compound heterozygous mutations inCOL7A1among families with severe recessive dystrophic epidermolysis bullosa in India - implications on diagnosis, prognosis and prenatal testing
2018 ◽
Vol 32
(12)
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pp. e433-e435
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2018 ◽
Vol 79
(3)
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pp. AB310
2017 ◽
Vol 60
(12)
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pp. 635-638
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2020 ◽
Vol 63
(1)
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pp. 103623
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2015 ◽
Vol 65
(10)
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pp. A1377
2015 ◽
Vol 240
(2)
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pp. 324-329
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2013 ◽
Vol 11
(1)
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pp. 284
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