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Results: 1-12 |
Results: 12
MOSAIC VARIEGATED ANEUPLOIDY WITH MULTIPLE CONGENITAL-ABNORMALITIES -HOMOZYGOSITY FOR TOTAL PREMATURE CHROMATID SEPARATION TRAIT
Authors: KAJII T KAWAI T TAKUMI T MISU H MABUCHI O TAKAHASHI Y TACHINO M NIHEI F IKEUCHI T
Citation: T. Kajii et al., MOSAIC VARIEGATED ANEUPLOIDY WITH MULTIPLE CONGENITAL-ABNORMALITIES -HOMOZYGOSITY FOR TOTAL PREMATURE CHROMATID SEPARATION TRAIT, American journal of medical genetics, 78(3), 1998, pp. 245-249
A RECURRENT TRANSLOCATION, T(16-21)(Q24-Q22), ASSOCIATED WITH ACUTE MYELOGENOUS LEUKEMIA - IDENTIFICATION BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: SHIMADA M OHTSUKA E SHIMIZU T MATSUMOTO T MATSUSHITA K TANIMOTO F KAJII T
Citation: M. Shimada et al., A RECURRENT TRANSLOCATION, T(16-21)(Q24-Q22), ASSOCIATED WITH ACUTE MYELOGENOUS LEUKEMIA - IDENTIFICATION BY FLUORESCENCE IN-SITU HYBRIDIZATION, Cancer genetics and cytogenetics, 96(2), 1997, pp. 102-105
INTERSTITIAL DELETION OF 8P - REPORT OF 2 PATIENTS AND REVIEW OF THE LITERATURE
Authors: TSUKAHARA M MURANO I AOKI Y KAJII T FURUKAWA S
Citation: M. Tsukahara et al., INTERSTITIAL DELETION OF 8P - REPORT OF 2 PATIENTS AND REVIEW OF THE LITERATURE, Clinical genetics, 48(1), 1995, pp. 41-45
MAPPING OF THE HUMAN GUANOSINE-MONOPHOSPHATE REDUCTASE GENE (GMPR) TOCHROMOSOME 6P23 BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: MURANO I TSUKAHARA M KAJII T YOSHIDA A
Citation: I. Murano et al., MAPPING OF THE HUMAN GUANOSINE-MONOPHOSPHATE REDUCTASE GENE (GMPR) TOCHROMOSOME 6P23 BY FLUORESCENCE IN-SITU HYBRIDIZATION, Genomics, 19(1), 1994, pp. 179-180
CONGENITAL HEART-DEFECTS IN AARSKOG SYNDROME
Authors: FERNANDEZ I TSUKAHARA M MITO H YOSHII H UCHIDA M MATSUO K KAJII T
Citation: I. Fernandez et al., CONGENITAL HEART-DEFECTS IN AARSKOG SYNDROME, American journal of medical genetics, 50(4), 1994, pp. 318-322
TRICHORHINOPHALANGEAL SYNDROME TYPE-III
Authors: KAJII T GONZALEZ IF MATSUURA S
Citation: T. Kajii et al., TRICHORHINOPHALANGEAL SYNDROME TYPE-III, American journal of medical genetics, 49(3), 1994, pp. 349-350
OCCIPITAL HORN SYNDROME - REPORT OF A PATIENT AND REVIEW OF THE LITERATURE
Authors: TSUKAHARA M IMAIZUMI K KAWAI S KAJII T
Citation: M. Tsukahara et al., OCCIPITAL HORN SYNDROME - REPORT OF A PATIENT AND REVIEW OF THE LITERATURE, Clinical genetics, 45(1), 1994, pp. 32-35
2 JAPANESE CASES WITH MICROCEPHALIC PRIMORDIAL DWARFISM - CLASSICAL SECKEL SYNDROME AND OSTEODYSPLASTIC PRIMORDIAL DWARFISM TYPE-II
Authors: SUGIO Y TSUKAHARA M KAJII T
Citation: Y. Sugio et al., 2 JAPANESE CASES WITH MICROCEPHALIC PRIMORDIAL DWARFISM - CLASSICAL SECKEL SYNDROME AND OSTEODYSPLASTIC PRIMORDIAL DWARFISM TYPE-II, JPN J HUM G, 38(2), 1993, pp. 209-217
MIDKINE GENE (MDK), A GENE FOR PRENATAL DIFFERENTIATION AND NEUROREGULATION, MAPS TO BAND-11P11.2 BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: KANAME T KUWANO A MURANO I UEHARA K MURAMATSU T KAJII T
Citation: T. Kaname et al., MIDKINE GENE (MDK), A GENE FOR PRENATAL DIFFERENTIATION AND NEUROREGULATION, MAPS TO BAND-11P11.2 BY FLUORESCENCE IN-SITU HYBRIDIZATION, Genomics, 17(2), 1993, pp. 514-515
MAPPING BASIGIN (BSG), A MEMBER OF THE IMMUNOGLOBULIN SUPERFAMILY, TO19P13.3
Authors: KANAME T MIYAUCHI T KUWANO A MATSUDA Y MURAMATSU T KAJII T
Citation: T. Kaname et al., MAPPING BASIGIN (BSG), A MEMBER OF THE IMMUNOGLOBULIN SUPERFAMILY, TO19P13.3, Cytogenetics and cell genetics, 64(3-4), 1993, pp. 195-197
PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY DIRECT-DETECTION OF THE DYNAMIC MUTATION DUE TO AN UNSTABLE DNA-SEQUENCE
Authors: YAMAUCHI M NAGATA S SEKI N TOYAMA Y HARADA N NIIKAWA N MASUNO I KAJII T HORI T
Citation: M. Yamauchi et al., PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY DIRECT-DETECTION OF THE DYNAMIC MUTATION DUE TO AN UNSTABLE DNA-SEQUENCE, Clinical genetics, 44(4), 1993, pp. 169-172
DICENTRIC Y-CHROMOSOME IN AZOOSPERMIC MALES
Authors: TAKIHARA H TSUKAHARA M BABA Y NAITO K KAJII T
Citation: H. Takihara et al., DICENTRIC Y-CHROMOSOME IN AZOOSPERMIC MALES, British Journal of Urology, 71(5), 1993, pp. 596-599
Risultati: 1-12 |