AAAAAA
Results:
1-14
|
Results: 14
Authors:
LIU XZ
NEWTON VE
STEEL KP
BROWN SDM
Citation: Xz. Liu et al., IDENTIFICATION OF A NEW MUTATION OF THE MYOSIN-VII HEAD REGION IN USHER-SYNDROME TYPE-1, Human mutation, 10(2), 1997, pp. 168-170
Authors:
READ AP
NEWTON VE
Citation: Ap. Read et Ve. Newton, WAARDENBURG-SYNDROME, Journal of Medical Genetics, 34(8), 1997, pp. 656-665
Authors:
LIU XZ
NEWTON VE
Citation: Xz. Liu et Ve. Newton, DISTORTION-PRODUCT EMISSIONS IN NORMAL-HEARING AND LOW-FREQUENCY HEARING-LOSS CARRIERS OF GENES FOR WAARDENBURGS-SYNDROME, The Annals of otology, rhinology & laryngology, 106(3), 1997, pp. 220-225
Authors:
BROWN KA
JANJUA AH
KARBANI G
PARRY G
NOBLE A
CROCKFORD G
BISHOP DT
NEWTON VE
MARKHAM AF
MUELLER RF
Citation: Ka. Brown et al., LINKAGE STUDIES OF NON-SYNDROMIC RECESSIVE DEAFNESS (NSRD) IN A FAMILY ORIGINATING FROM THE MIRPUR REGION OF PAKISTAN MAPS DFNB1 CENTROMERIC TO D13S175 (VOL 5, PG 169, 1996), Human molecular genetics, 5(5), 1996, pp. 710-710
Authors:
BROWN KA
JANJUA AH
KARBANI G
PARRY G
NOBLE A
CROCKFORD G
BISHOP DT
NEWTON VE
MARKHAM AF
MUELLER RF
Citation: Ka. Brown et al., LINKAGE STUDIES OF NON-SYNDROMIC RECESSIVE DEAFNESS (NSRD) IN A FAMILY ORIGINATING FROM THE MIRPUR REGION OF PAKISTAN MAPS DFNB1 CENTROMERIC TO D13S175, Human molecular genetics, 5(1), 1996, pp. 169-173
Authors:
NEARY WJ
NEWTON VE
LAOIDEKEMP SN
RAMSDEN RT
GRIFFITH G
EVANS DG
HARRIS R
STRACHAN T
Citation: Wj. Neary et al., A CLINICAL, GENETIC AND AUDIOLOGICAL STUDY OF PATIENTS AND FAMILIES WITH UNILATERAL VESTIBULAR SCHWANNOMAS .1. CLINICAL-FEATURES OF NEUROFIBROMATOSIS IN PATIENTS WITH UNILATERAL VESTIBULAR SCHWANNOMAS, Journal of Laryngology and Otology, 110(7), 1996, pp. 634-640
Authors:
NEARY WJ
NEWTON VE
LAOIDEKEMP SN
RAMSDEN RT
HILLIER VF
KAN SW
Citation: Wj. Neary et al., A CLINICAL, GENETIC AND AUDIOLOGICAL STUDY OF PATIENTS AND FAMILIES WITH UNILATERAL VESTIBULAR SCHWANNOMAS .2. AUDIOLOGICAL FINDINGS IN 93 PATIENTS WITH UNILATERAL VESTIBULAR SCHWANNOMAS, Journal of Laryngology and Otology, 110(12), 1996, pp. 1120-1128
Authors:
TASSABEHJI M
NEWTON VE
LIU XZ
BRADY A
DONNAI D
KRAJEWSKAWALASEK M
MURDAY V
NORMAN A
OBERSZTYN E
REARDON W
RICE JC
TREMBATH R
WIEACKER P
WHITEFORD M
WINTER R
READ AP
Citation: M. Tassabehji et al., THE MUTATIONAL SPECTRUM IN WAARDENBURG SYNDROME, Human molecular genetics, 4(11), 1995, pp. 2131-2137
Authors:
LIU XZ
NEWTON VE
READ AP
Citation: Xz. Liu et al., WAARDENBURG SYNDROME TYPE-II - PHENOTYPIC FINDINGS AND DIAGNOSTIC-CRITERIA, American journal of medical genetics, 55(1), 1995, pp. 95-100
Authors:
READ AP
NEWTON VE
TASSABEHJI M
Citation: Ap. Read et al., PAX3 AND MITF MUTATIONS IN AUDITORY-PIGMENTARY SYNDROMES, American journal of human genetics, 57(4), 1995, pp. 1304-1304
Authors:
TASSABEHJI M
NEWTON VE
READ AP
Citation: M. Tassabehji et al., WAARDENBURG SYNDROME TYPE-2 CAUSED BY MUTATIONS IN THE HUMAN MICROPHTHALMIA (MITF) GENE, Nature genetics, 8(3), 1994, pp. 251-255
Authors:
HUGHES AE
NEWTON VE
LIU XZ
READ AP
Citation: Ae. Hughes et al., A GENE FOR WAARDENBURG SYNDROME TYPE-2 MAPS CLOSE TO THE HUMAN HOMOLOG OF THE MICROPHTHALMIA GENE AT CHROMOSOME 3P12-P14.1, Nature genetics, 7(4), 1994, pp. 509-512
Authors:
TASSABEHJI M
NEWTON VE
LEVERTON K
TURNBULL K
SEEMANOVA E
KUNZE J
SPERLING K
STRACHAN T
READ AP
Citation: M. Tassabehji et al., PAX3 GENE STRUCTURE AND MUTATIONS - CLOSE ANALOGIES BETWEEN WAARDENBURG SYNDROME AND THE SPLOTCH MOUSE, Human molecular genetics, 3(7), 1994, pp. 1069-1074
Authors:
MORRIS DJ
SIMS D
CHISWICK M
DAS VK
NEWTON VE
Citation: Dj. Morris et al., SYMPTOMATIC CONGENITAL CYTOMEGALOVIRUS-INFECTION AFTER MATERNAL RECURRENT INFECTION, The Pediatric infectious disease journal, 13(1), 1994, pp. 61-64
Risultati:
1-14
|