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Results:
1-22
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Results: 22
Authors:
OGATA T
WAKUI K
MUROYA K
OHASHI H
MATSUO N
BROWN DM
ISHII T
FUKUSHIMA Y
Citation: T. Ogata et al., MICROPHTHALMIA WITH LINEAR SKIN DEFECTS SYNDROME IN A MOSAIC FEMALE INFANT WITH MONOSOMY FOR THE XP22 REGION - MOLECULAR ANALYSIS OF THE XP22 BREAKPOINT AND THE X-INACTIVATION PATTERN, Human genetics, 103(1), 1998, pp. 51-56
Authors:
WAKUI K
AOYAMA T
UCHIYAMA A
HASHIMOTO T
FUKUSHIMA Y
Citation: K. Wakui et al., ASSIGNMENT OF HUMAN FATTY-ACID-COENZYME-A LIGASE, VERY LONG-CHAIN-1 GENE (FACVL1) TO HUMAN-CHROMOSOME BAND 15Q21.2 BY FLUORESCENCE IN-SITU HYBRIDIZATION, Cytogenetics and cell genetics, 81(3-4), 1998, pp. 292-293
Authors:
IMAMURA K
TONOKI H
WAKUI K
FUKUSHIMA Y
SASAKI S
YAUSDA K
TAKEKOSHI Y
TOCHIMARU H
Citation: K. Imamura et al., 4Q33-QTER DELETION AND ABSORPTIVE HYPERCALCIURIA - REPORT OF 2 UNRELATED GIRLS, American journal of medical genetics, 78(1), 1998, pp. 52-54
Authors:
KUBOTA T
SAKURAI A
ARAKAWA K
SHIMAZU M
WAKUI K
FURIHATA K
FUKUSHIMA Y
Citation: T. Kubota et al., IDENTIFICATION OF 2 NOVEL MUTATIONS IN THE OCRL1 GENE IN JAPANESE FAMILIES WITH LOWE-SYNDROME, Clinical genetics, 54(3), 1998, pp. 199-202
Authors:
ORII KE
AOYAMA T
WAKUI K
FUKUSHIMA Y
MIYAJIMA H
YAMAGUCHI S
ORII T
KONDO N
HASHIMOTO T
Citation: Ke. Orii et al., GENOMIC AND MUTATIONAL ANALYSIS OF THE MITOCHONDRIAL TRIFUNCTIONAL PROTEIN BETA-SUBUNIT (HADHB) GENE IN PATIENTS WITH TRIFUNCTIONAL PROTEIN-DEFICIENCY, Human molecular genetics, 6(8), 1997, pp. 1215-1224
Authors:
NAGAI M
SAKAKIBARA J
WAKUI K
FUKUSHIMA Y
IGARASHI S
TSUJI S
ARAKAWA M
ONO T
Citation: M. Nagai et al., LOCALIZATION OF THE SQUALENE EPOXIDASE GENE (SQLE) TO HUMAN-CHROMOSOME REGION 8Q24.1, Genomics, 44(1), 1997, pp. 141-143
Authors:
AOYAMA T
WAKUI K
ORII KE
HASHIMOTO T
FUKUSHIMA Y
Citation: T. Aoyama et al., FLUORESCENCE IN-SITU HYBRIDIZATION MAPPING OF THE ALPHA-SUBUNIT AND BETA-SUBUNIT (HADHA AND HADHB) OF HUMAN MITOCHONDRIAL FATTY-ACID BETA-OXIDATION MULTIENZYME COMPLEX TO 2P23 AND THEIR EVOLUTION, Cytogenetics and cell genetics, 79(3-4), 1997, pp. 221-224
Authors:
HASEGAWA T
HASEGAWA Y
ASO T
KOTO S
NAGAI T
TSUCHIYA Y
KIM KC
OHASHI H
WAKUI K
FUKUSHIMA Y
Citation: T. Hasegawa et al., HDR SYNDROME (HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, RENAL DYSPLASIA) ASSOCIATED WITH DEL(10)(P13), American journal of medical genetics, 73(4), 1997, pp. 416-418
Authors:
KIM KC
WAKUI K
YAMAGISHI A
OHNO T
SATO M
IMAIZUMI S
AIHARA T
FUKUSHIMA Y
OHASHI H
Citation: Kc. Kim et al., TETRAMELIC MIRROR-IMAGE POLYDACTYLY AND A DE-NOVO BALANCED TRANSLOCATION BETWEEN 2P23.3 AND 14Q13, American journal of medical genetics, 68(1), 1997, pp. 70-73
Authors:
WAKUI K
KUBOTA T
SUZUMORI K
OGATA T
LEDBETTER DH
FUKUSHIMA Y
Citation: K. Wakui et al., ADVANCED DIAGNOSIS OF CHROMOSOME-ABERRATIONS BY FISH ANALYSIS WITH TELOMERIC PROBES, American journal of human genetics, 61(4), 1997, pp. 810-810
Authors:
AOYAMA T
WAKUI K
FUKUSHIMA Y
ORII KO
HASHIMOTO T
Citation: T. Aoyama et al., ASSIGNMENT OF THE HUMAN MITOCHONDRIAL VERY-LONG-CHAIN ACYL-COA DEHYDROGENASE GENE (LCACD) TO 17P13 BY IN-SITU HYBRIDIZATION, Genomics, 37(1), 1996, pp. 144-145
Authors:
WAKUI K
OHASHI H
YAMAGISHI A
HAMANO S
NARA T
ISHIKIRIYAMA S
NAKAMURA Y
FUKUSHIMA Y
Citation: K. Wakui et al., INTERSTITIAL DUPLICATION 8Q22-Q24 - REPORT OF A CASE PROVEN BY FISH WITH MAPPED COSMID PROBES, American journal of medical genetics, 65(1), 1996, pp. 36-39
Authors:
YAMAMOTO T
WAKUI K
KOBAYASHI M
Citation: T. Yamamoto et al., HEMANGIOBLASTOMA IN THE CEREBELLAR VERMIS - A CASE-REPORT, Acta cytologica, 40(2), 1996, pp. 346-350
Authors:
SHIMURA E
WAKUI K
TAKAMOTO S
Citation: E. Shimura et al., THE EFFECTS OF ALKALI-METAL IONS AND ALKA LINE-EARTH METAL-IONS ON THE ADDUCT FORMATION OF THIOCYANATO-N COBALTATE(II) COMPLEXES WITH NONIONIC SURFACTANT, Nippon kagaku kaishi, (2), 1995, pp. 119-122
Authors:
FUKUSHIMA Y
OHASHI H
WAKUI K
NISHIMOTO H
SATO M
AIHARA T
Citation: Y. Fukushima et al., DE-NOVO APPARENTLY BALANCED RECIPROCAL TRANSLOCATION BETWEEN 5Q11.2 AND 17Q23 ASSOCIATED WITH KLIPPEL-FEIL ANOMALY AND TYPE A1 BRACHYDACTYLY, American journal of medical genetics, 57(3), 1995, pp. 447-449
Authors:
OHASHI H
KIN Y
IWASAKI M
OHNO T
SATO M
IMAIZUMI S
AIHARA T
YAMAGISHI A
WAKUI K
FUKUSHIMA Y
Citation: H. Ohashi et al., TETRAMELIC MIRROR-IMAGE LIKE POLYDACTYLY AND DE-NOVO BALANCED AUTOSOMAL TRANSLOCATION [46,XY,T(2-14)(P23.2-Q13)], American journal of human genetics, 57(4), 1995, pp. 543-543
Authors:
WAKUI K
TAKAHATA Y
KAIZUMA N
Citation: K. Wakui et al., EFFECT OF ABSCISIC-ACID AND HIGH OSMOTICUM CONCENTRATION ON THE INDUCTION OF DESICCATION TOLERANCE IN MICROSPORE-DERIVED EMBRYOS OF CHINESE-CABBAGE (BRASSICA-CAMPESTRIS L), Ikushugaku Zasshi, 44(1), 1994, pp. 29-34
Authors:
OHASHI H
WAKUI K
OGAWA K
OKANO T
NIIKAWA N
FUKUSHIMA Y
Citation: H. Ohashi et al., A STABLE ACENTRIC MARKER CHROMOSOME - POSSIBLE EXISTENCE OF AN INTERCALARY ANCIENT CENTROMERE AT DISTAL 8P, American journal of human genetics, 55(6), 1994, pp. 1202-1208
Authors:
WAKUI K
TAKAMOTO S
Citation: K. Wakui et S. Takamoto, ADDUCTS OF HEAVY-METAL THIOCYANATO-N COMP LEXES WITH NONIONIC SURFACTANT .2. ADDUCTS FORMATION OF VARIOUS HEAVY-METAL THIOCYANATO-N-COMPLEXES WITH NONIONIC SURFACTANT, Nippon kagaku kaishi, (12), 1993, pp. 1320-1327
Authors:
FUKUSHIMA Y
HOOVERS J
MANNENS M
WAKUI K
OHASHI H
OHNO T
UEOKA Y
NIIKAWA N
Citation: Y. Fukushima et al., DETECTION OF A CRYPTIC PARACENTRIC INVERSION WITHIN BAND-11P13 IN FAMILIAL ANIRIDIA BY FLUORESCENCE INSITU HYBRIDIZATION, Human genetics, 91(3), 1993, pp. 205-209
Authors:
OHASHI H
WAKUI K
SEKI K
NIIKAWA N
FUKUSHIMA Y
Citation: H. Ohashi et al., PARTIAL CAT EYE SYNDROME AND SUPERNUMERARY SMALL RING CHROMOSOME-22 DETECTED BY MICRODISSECTION-CHROMOSOME PAINTING METHOD, American journal of human genetics, 53(3), 1993, pp. 586-586
Authors:
FUKUSHIMA Y
OHASHI H
WAKUI K
FUJIWARA M
NAKAMURA Y
OGAWA K
Citation: Y. Fukushima et al., POLYSPLENIA SYNDROME AND PARACENTRIC INVERSION OF CHROMOSOME-11 [46,XX,INV(11)(Q13Q25)], American journal of human genetics, 53(3), 1993, pp. 1543-1543
Risultati:
1-22
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