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Results:
1-16
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Results: 16
Authors:
Kosaki, K
Suzuki, T
Kosaki, R
Yoshihashi, H
Itoh, M
Goto, Y
Matsuo, N
Citation: K. Kosaki et al., Human homolog of the mouse imprinted gene Impact resides at the pericentric region of chromosome 18 within the critical region for bipolar affective disorder, MOL PSYCHI, 6(1), 2001, pp. 87-91
Authors:
Nishimura, G
Manabe, N
Kosaki, K
Haga, N
Ohashi, H
Nakamura, K
Ikegawa, S
Citation: G. Nishimura et al., Spondylar dysplasia in type X collagenopathy, PEDIAT RAD, 31(2), 2001, pp. 76-80
Authors:
Kosaki, K
Yoshihashi, H
Ohashi, Y
Kosaki, R
Suzuki, T
Matsuo, N
Citation: K. Kosaki et al., Fluorescence-based DHPLC for allelic quantification by single-nucleotide primer extension, J BIOCH BIO, 47(1-2), 2001, pp. 111-119
Authors:
Maeyama, K
Kosaki, R
Yoshihashi, H
Casey, B
Kosaki, K
Citation: K. Maeyama et al., Mutation analysis of left-right axis determining genes in NOD and ICR, strains susceptible to maternal diabetes, TERATOLOGY, 63(3), 2001, pp. 119-126
Authors:
Ishii, T
Sato, S
Kosaki, K
Sasaki, G
Muroya, K
Ogata, T
Matsuo, N
Citation: T. Ishii et al., Micropenis and the AR gene: Mutation and CAG repeat-length analysis, J CLIN END, 86(11), 2001, pp. 5372-5378
Authors:
Kosaki, R
Ohashi, H
Yoshihashi, H
Suzuki, T
Kosaki, K
Citation: R. Kosaki et al., A de novo mutation (R279C) in the P63 gene in a patient with EEC syndrome, CLIN GENET, 60(4), 2001, pp. 314-315
Authors:
Kosaki, K
Shimasaki, N
Fukushima, H
Hara, M
Ogata, T
Matsuo, N
Citation: K. Kosaki et al., Female patient showing hypohidrotic ectodermal dysplasia and immunodeficiency (HED-ID), AM J HU GEN, 69(3), 2001, pp. 664-665
Authors:
Yoshihashi, H
Maeyama, K
Kosaki, R
Ogata, T
Tsukahara, M
Goto, YI
Hata, J
Matsuo, N
Smith, RJ
Kosaki, K
Citation: H. Yoshihashi et al., Conflicting reports of imprinting status of human GRB10 in developing brain: How reliable are somatic cell hybrids for predicting allelic origin of expression? Reply, AM J HU GEN, 68(2), 2001, pp. 544-545
Authors:
Matsuo, M
Muroya, K
Nanao, K
Hasegawa, Y
Terasaki, H
Kosaki, K
Ogata, T
Citation: M. Matsuo et al., Mother and daughter with 45,X/46,X,r(X) (p22.3q28) and mental retardation:Analysis of the X-inactivation patterns, AM J MED G, 91(4), 2000, pp. 267-272
Authors:
Yoshihashi, H
Maeyama, K
Kosaki, R
Ogata, T
Tsukahara, M
Goto, Y
Hata, J
Matsuo, N
Smith, RJ
Kosaki, K
Citation: H. Yoshihashi et al., Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome, AM J HU GEN, 67(2), 2000, pp. 476-482
Authors:
Kosaki, K
Kosaki, R
Craigen, WJ
Matsuo, N
Citation: K. Kosaki et al., Isoform-specific imprinting of the human PEG1/MEST gene, AM J HU GEN, 66(1), 2000, pp. 309-312
Authors:
Suzuki, H
Delano, FA
Jamshidi, N
Katz, D
Mori, M
Kosaki, K
Gottlieb, RA
Ishii, H
Schmid-Schonbein, GW
Citation: H. Suzuki et al., Enhanced DNA fragmentation in the thymus of spontaneously hypertensive rats, AM J P-HEAR, 45(6), 1999, pp. H2135-H2140
Authors:
Matsuo, M
Muroya, K
Kosaki, K
Ishii, T
Fukushima, Y
Anzo, M
Ogata, T
Citation: M. Matsuo et al., Random x-inactivation in a girl with duplication Xp11.21-p21.3: Report of a patient and review of the literature, AM J MED G, 86(1), 1999, pp. 44-50
Authors:
Kosaki, R
Gebbia, M
Kosaki, K
Lewin, M
Bowers, P
Towbin, JA
Casey, B
Citation: R. Kosaki et al., Left-right axis malformations associated with mutations in ACVR2B, the gene for human activin receptor type IIB, AM J MED G, 82(1), 1999, pp. 70-76
Authors:
Del Campo, M
Kosaki, K
Bennett, FC
Jones, KL
Citation: M. Del Campo et al., Developmental delay in fetal aminopterin methotrexate syndrome, TERATOLOGY, 60(1), 1999, pp. 10-12
Authors:
Kosaki, K
Bassi, MT
Kosaki, R
Lewin, M
Belmont, J
Schauer, G
Casey, B
Citation: K. Kosaki et al., Characterization and mutation analysis of human LEFTY A and LEFTY B, homologues of murine genes implicated in left-right axis development, AM J HU GEN, 64(3), 1999, pp. 712-721
Risultati:
1-16
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