GENETIC CAUSES OF NON-SYNDROMIC HEARING LOSS

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SKVORAK G.A.B.; MORTON C.C.

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Journal Paper

Paper Information

Journal: CURRENT OPINION IN PEDIATRICS Year:1999 | Volume:11 | Issue:- Page(s): 551-557

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Information Journal Paper

Title

GENETIC CAUSES OF NON-SYNDROMIC HEARING LOSS

Author(s)

SKVORAK G.A.B. | MORTON C.C. | Issue Writer Certificate

Keywords

Not Registered.

Abstract

Cites

DEAFNESS-ASSOCIATED CONNEXIN 26 GENE (GJB2) MUTATIONS IN IRANIAN POPULATION
FREQUENCIES OF MUTATIONS IN THE CONNEXIN 26 GENE (GJB2) IN TWO POPULATIONS OF IRAN (TEHRAN AND TABRIZ)
TWO NOVEL MUTATIONS AND PREDOMINANT 35DELG MUTATION IN THE CONNEXIN 26 GENE (GJB2) IN IRANIAN POPULATIONS
REPORT OF A NEW MUTATION AND FREQUENCY OF CONNEXIN 26 GENE (GJB2) MUTATIONS IN PATIENTS FROM THREE PROVINCES OF IRAN

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APA: Copy

SKVORAK, G.A.B., & MORTON, C.C.. (1999). GENETIC CAUSES OF NON-SYNDROMIC HEARING LOSS. CURRENT OPINION IN PEDIATRICS, 11(-), 551-557. SID. https://sid.ir/paper/545172/en

Vancouver: Copy

SKVORAK G.A.B., MORTON C.C.. GENETIC CAUSES OF NON-SYNDROMIC HEARING LOSS. CURRENT OPINION IN PEDIATRICS[Internet]. 1999;11(-):551-557. Available from: https://sid.ir/paper/545172/en

IEEE: Copy

G.A.B. SKVORAK, and C.C. MORTON, “GENETIC CAUSES OF NON-SYNDROMIC HEARING LOSS,” CURRENT OPINION IN PEDIATRICS, vol. 11, no. -, pp. 551–557, 1999, [Online]. Available: https://sid.ir/paper/545172/en

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