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Results: 1-10 |
Results: 10
REFINED PHYSICAL AND PARTIAL TRANSCRIPT MAP OF THE USHER-SYNDROME TYPE-III REGION
Authors: JOENSUU T LEHESJOKI AE DELACHAPELLE A SANKILA EM
Citation: T. Joensuu et al., REFINED PHYSICAL AND PARTIAL TRANSCRIPT MAP OF THE USHER-SYNDROME TYPE-III REGION, European journal of human genetics, 6, 1998, pp. 4083-4083
MOLECULAR STUDIES IN FINNISH PATIENTS WITH FAMILIAL JUVENILE NEPHRONOPHTHISIS EXCLUDE A FOUNDER EFFECT AND SUPPORT A COMMON MUTATION CAUSING MECHANISM
Authors: ALAMELLO S SANKILA EM KOSKIMIES O DELACHAPELLE A KAARIAINEN H
Citation: S. Alamello et al., MOLECULAR STUDIES IN FINNISH PATIENTS WITH FAMILIAL JUVENILE NEPHRONOPHTHISIS EXCLUDE A FOUNDER EFFECT AND SUPPORT A COMMON MUTATION CAUSING MECHANISM, Journal of Medical Genetics, 35(4), 1998, pp. 279-283
MOLECULAR STUDIES IN FINNISH PATIENTS WITH FAMILIAL JUVENILE NEPHRONOPHTHISIS EXCLUDE A FOUNDER EFFECT AND SUPPORT A COMMON MUTATION CAUSING MECHANISM
Authors: ALAMELLO S SANKILA EM KOSKIMIES O DELACHAPELLE A KAARIAINEN H
Citation: S. Alamello et al., MOLECULAR STUDIES IN FINNISH PATIENTS WITH FAMILIAL JUVENILE NEPHRONOPHTHISIS EXCLUDE A FOUNDER EFFECT AND SUPPORT A COMMON MUTATION CAUSING MECHANISM, American journal of human genetics, 61(4), 1997, pp. 1543-1543
REFINED MAPPING OF THE USHER-SYNDROME TYPE-III LOCUS ON CHROMOSOME-3,EXCLUSION OF CANDIDATE GENES, AND IDENTIFICATION OF THE PUTATIVE MOUSE HOMOLOGOUS REGION
Authors: JOENSUU T BLANCO G PAKARINEN L SISTONEN P KAARIAINEN H BROWN S DELACHAPELLE A SANKILA EM
Citation: T. Joensuu et al., REFINED MAPPING OF THE USHER-SYNDROME TYPE-III LOCUS ON CHROMOSOME-3,EXCLUSION OF CANDIDATE GENES, AND IDENTIFICATION OF THE PUTATIVE MOUSE HOMOLOGOUS REGION, Genomics, 38(3), 1996, pp. 255-263
REPORT OF THE 6TH INTERNATIONAL WORKSHOP ON HUMAN-CHROMOSOME-3 MAPPING 1995 - HELD ON 23-24 OCTOBER 1995 - MINNEAPOLIS, MINNESOTA
Authors: NAYLOR SL CARRITT B BOILEAU C BEROUD C ALEXANDER C ALLDERDICE P ALIMOV A ASHWORTH T BONIFAS J BUGERT P BUYS CHCM CHIPPERFIELD MA DENG G DRABKIN H GEMMILL RM GROMPE M JOENSUU T JONASDOTTIR A GIZATULLIN R KROIS L LEACH RJ LOTT ST KILLARY A MARTINSSON T MESSIAEN L OCONNELL P OPALKA B PLAETKE R SANKILA EM SMITH DI STRACHEN T VANDENBERG A ZABAROVSKY E
Citation: Sl. Naylor et al., REPORT OF THE 6TH INTERNATIONAL WORKSHOP ON HUMAN-CHROMOSOME-3 MAPPING 1995 - HELD ON 23-24 OCTOBER 1995 - MINNEAPOLIS, MINNESOTA, Cytogenetics and cell genetics, 72(4), 1996, pp. 255-267
ASSIGNMENT OF AN USHER SYNDROME TYPE-III (USH3) GENE TO CHROMOSOME 3Q
Authors: SANKILA EM PAKARINEN L KAARIAINEN H AITTOMAKI K KARJALAINEN S SISTONEN P DELACHAPELLE A
Citation: Em. Sankila et al., ASSIGNMENT OF AN USHER SYNDROME TYPE-III (USH3) GENE TO CHROMOSOME 3Q, Human molecular genetics, 4(1), 1995, pp. 93-98
MUTATION IN THE FOLLICLE-STIMULATING-HORMONE RECEPTOR GENE CAUSES HEREDITARY HYPERGONADOTROPIC OVARIAN FAILURE
Authors: AITTOMAKI K LUCENA JLD PAKARINEN P SISTONEN P TAPANAINEN J GROMOLL J KASKIKARI R SANKILA EM LEHVASLAIHO H ENGEL AR NIESCHLAG E HUHTANIEMI I DELACHAPELLE A
Citation: K. Aittomaki et al., MUTATION IN THE FOLLICLE-STIMULATING-HORMONE RECEPTOR GENE CAUSES HEREDITARY HYPERGONADOTROPIC OVARIAN FAILURE, Cell, 82(6), 1995, pp. 959-968
REFINED MAPPING OF THE USHER SYNDROME TYPE-III (USH3) LOCUS
Authors: JOENSUU TH PAKARINEN L KAARIAINEN H DELACHAPELLE A SANKILA EM
Citation: Th. Joensuu et al., REFINED MAPPING OF THE USHER SYNDROME TYPE-III (USH3) LOCUS, American journal of human genetics, 57(4), 1995, pp. 1115-1115
MUTATION SPECTRUM IN THE CHM GENE OF DANISH AND SWEDISH CHOROIDEREMIAPATIENTS
Authors: VANBOKHOVEN H SCHWARTZ M ANDREASSON S VANDENHURK JAJM BOGERD L JAY M RUTHER K JAY B PAWLOWITZKI IH SANKILA EM WRIGHT A ROPERS HH ROSENBERG T CREMERS FPM
Citation: H. Vanbokhoven et al., MUTATION SPECTRUM IN THE CHM GENE OF DANISH AND SWEDISH CHOROIDEREMIAPATIENTS, Human molecular genetics, 3(7), 1994, pp. 1047-1051
GENETIC-LINKAGE STUDIES IN USHER SYNDROME TYPE-3
Authors: SANKILA EM PAKARINEN L SIMOLA KOJ KAARIAINEN H DELACHAPELLE A
Citation: Em. Sankila et al., GENETIC-LINKAGE STUDIES IN USHER SYNDROME TYPE-3, American journal of human genetics, 53(3), 1993, pp. 1712-1712
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