CONNEXIN-26-ASSOCIATED DEAFNESS: PHENOTYPIC VARIABILITY AND PROGRESSION OF HEARING LOSS

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CHAN D.K.; SCHRIJVER I.

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Journal Paper

Paper Information

Journal: GENETICS IN MEDICINE : OFFICIAL JOURNAL OF THE AMERICAN COLLEGE OF MEDICAL GENETICS Year:2010 | Volume:12 | Issue:3 Page(s): 174-181

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Information Journal Paper

Title

CONNEXIN-26-ASSOCIATED DEAFNESS: PHENOTYPIC VARIABILITY AND PROGRESSION OF HEARING LOSS

Author(s)

CHAN D.K. | SCHRIJVER I. | Issue Writer Certificate

Keywords

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Abstract

Cites

A NOVEL COMPOUND HETEROZYGOUS MUTATION (35DELG, 363DELC) IN THE CONNEXIN 26 GENE CAUSES NON-SYNDROMIC AUTOSOMAL RECESSIVE HEARING LOSS (CASE REPORT)

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APA: Copy

CHAN, D.K., & SCHRIJVER, I.. (2010). CONNEXIN-26-ASSOCIATED DEAFNESS: PHENOTYPIC VARIABILITY AND PROGRESSION OF HEARING LOSS. GENETICS IN MEDICINE : OFFICIAL JOURNAL OF THE AMERICAN COLLEGE OF MEDICAL GENETICS, 12(3), 174-181. SID. https://sid.ir/paper/663406/en

Vancouver: Copy

CHAN D.K., SCHRIJVER I.. CONNEXIN-26-ASSOCIATED DEAFNESS: PHENOTYPIC VARIABILITY AND PROGRESSION OF HEARING LOSS. GENETICS IN MEDICINE : OFFICIAL JOURNAL OF THE AMERICAN COLLEGE OF MEDICAL GENETICS[Internet]. 2010;12(3):174-181. Available from: https://sid.ir/paper/663406/en

IEEE: Copy

D.K. CHAN, and I. SCHRIJVER, “CONNEXIN-26-ASSOCIATED DEAFNESS: PHENOTYPIC VARIABILITY AND PROGRESSION OF HEARING LOSS,” GENETICS IN MEDICINE : OFFICIAL JOURNAL OF THE AMERICAN COLLEGE OF MEDICAL GENETICS, vol. 12, no. 3, pp. 174–181, 2010, [Online]. Available: https://sid.ir/paper/663406/en

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