Authors:
MAW M
KUMARAMANICKAVEL G
KAR B
JOHN S
BRIDGES R
DENTON M
Citation: M. Maw et al., 2 INDIAN SIBLINGS WITH OGUCHI-DISEASE ARE HOMOZYGOUS FOR AN ARRESTIN MUTATION ENCODING PREMATURE TERMINATION, Human mutation, 1998, pp. 317-319
Authors:
HYSLOP SJ
JAMES AM
MAW M
FISCHELGHODSIAN N
MURPHY MP
Citation: Sj. Hyslop et al., THE EFFECT ON MITOCHONDRIAL-FUNCTION OF THE TRNA(SER(UCN)) COI A7445GMTDNA POINT MUTATION ASSOCIATED WITH MATERNALLY-INHERITED SENSORINEURAL DEAFNESS/, Biochemistry and molecular biology international, 42(3), 1997, pp. 567-575
Authors:
MAW M
KAR B
BISWAS J
BISWAS P
NANCARROW D
BRIDGES R
KUMARAMANICKAVEL G
DENTON M
BADRINATH SS
Citation: M. Maw et al., LINKAGE OF BLEPHAROPHIMOSIS SYNDROME IN A LARGE INDIAN PEDIGREE TO CHROMOSOME 7P, Human molecular genetics, 5(12), 1996, pp. 2049-2054
Authors:
JINNO Y
IKEDA Y
YUN K
MAW M
MASUZAKI H
FUKUDA H
INUZUKA K
FUJISHITA A
OHTANI Y
OKIMOTO T
ISHIMARU TS
NIIKAWA N
Citation: Y. Jinno et al., ESTABLISHMENT OF FUNCTIONAL IMPRINTING OF THE H19 GENE IN HUMAN DEVELOPING PLACENTAE, Nature genetics, 10(3), 1995, pp. 318-324
Authors:
FUCHS S
NAKAZAWA M
MAW M
TAMAI M
OGUCHI Y
GAL A
Citation: S. Fuchs et al., A HOMOZYGOUS 1-BASE PAIR DELETION IN THE ARRESTIN GENE IS A FREQUENT CAUSE OF OGUCHI DISEASE IN JAPANESE, Nature genetics, 10(3), 1995, pp. 360-362
Authors:
FISCHELGHODSIAN N
PREZANT TR
FOURNIER P
STEWART IA
MAW M
Citation: N. Fischelghodsian et al., MITOCHONDRIAL MUTATION ASSOCIATED WITH NONSYNDROMIC DEAFNESS, American journal of otolaryngology, 16(6), 1995, pp. 403-408