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Molecular and clinical studies of X-linked deafness among Pakistani families.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 10, p. 752, doi. 10.1038/jhg.2011.89
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- Article
Molecular and clinical studies of X-linked deafness among Pakistani families.
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- Journal of Human Genetics, 2011, v. 56, n. 7, p. 534, doi. 10.1038/jhg.2011.55
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- Article
Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani population.
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- Scientific Reports, 2017, p. 44185, doi. 10.1038/srep44185
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- Article
Identities and frequencies of variants in CYP1B1 causing primary congenital glaucoma in Pakistan.
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- Molecular Vision, 2019, v. 25, p. 144
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- Article
Delineating the Molecular and Phenotypic Spectrum of the CNGA3 -Related Cone Photoreceptor Disorder in Pakistani Families.
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- Genes, 2022, v. 13, n. 4, p. 617, doi. 10.3390/genes13040617
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- Article
Genetic Causes of Oculocutaneous Albinism in Pakistani Population.
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- Genes, 2021, v. 12, n. 4, p. 492, doi. 10.3390/genes12040492
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- Article
Identification and clinical characterization of Hermansky-Pudlak syndrome alleles in the Pakistani population.
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- Pigment Cell & Melanoma Research, 2016, v. 29, n. 2, p. 231, doi. 10.1111/pcmr.12438
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- Article
Identification and functional characterization of natural human melanocortin 1 receptor mutant alleles in Pakistani population.
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- Pigment Cell & Melanoma Research, 2015, v. 28, n. 6, p. 730, doi. 10.1111/pcmr.12400
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- Article