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FURTHER ELUCIDATION OF THE GENOMIC STRUCTURE OF PAX3, AND IDENTIFICATION OF 2 DIFFERENT POINT MUTATIONS WITHIN THE PAX3 HOMEOBOX THAT CAUSEWAARDENBURG SYNDROME TYPE-I IN 2 FAMILIES
Authors: LALWANI AK BRISTER JR FEX J GRUNDFAST KM PLOPLIS B SANAGUSTIN TB WILCOX ER
Citation: Ak. Lalwani et al., FURTHER ELUCIDATION OF THE GENOMIC STRUCTURE OF PAX3, AND IDENTIFICATION OF 2 DIFFERENT POINT MUTATIONS WITHIN THE PAX3 HOMEOBOX THAT CAUSEWAARDENBURG SYNDROME TYPE-I IN 2 FAMILIES, American journal of human genetics, 56(1), 1995, pp. 75-83
NEW NONSYNDROMIC X-LINKED SENSORINEURAL HEARING IMPAIRMENT LINKED TO XP21.2
Authors: LALWANI AK BRISTER JR FEX J GRUNDFAST KM PIKUS AT PLOPLIS B SANAGUSTIN T SKARKA H WILCOX ER
Citation: Ak. Lalwani et al., NEW NONSYNDROMIC X-LINKED SENSORINEURAL HEARING IMPAIRMENT LINKED TO XP21.2, American journal of human genetics, 55(4), 1994, pp. 685-694
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