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Yoshimitsu Fukushima

Veröffentlichungen von Yoshimitsu Fukushima zu Fukushima, Yoshimitsu ->
weitere Veröffentlichungen von Yoshimitsu Fukushima:
A case of an interstitial deletion of the long arm of chromosome 5: 46,XX,del(5)(q15q22) (1984)
The Prader-Willi syndrome and interstitial deletion of chromosome 15: High-resolution chromosome analyses of 14 patients with the Prader-Willi syndrome and of 5 suspected infants (1984)
Activity and antigen of coagulation factors VII and X in five patients with abnormal chromosome 13 (1987)
Partial distal 12q trisomy with arachnoid cyst (1987)
Familial retinoblastoma (mother and son) with 13q14 deletion (1987)
Two unrelated cases of single maxillary central incisor with 7q terminal deletion (1990)
The Costello syndrome: Are nasal papillomata essential? (1993)
Mutations of the fibroblast growth factor receptor-3 gene in one familial and six sporadic cases of achondroplasia in Japanese patients (1995)
Recurrence of osteogenesis imperfecta because of paternal mosaicism: Gly862→Ser substitution in a type I collagen gene (COL1A1) (1995)
False aneurysm of the popliteal artery treated successfully by surgery: Report of two cases (1997)
Predisposition to autoimmune thyroiditis in ring chromosome 18 syndrome (1984)
De novo interstitial deletion of 4q[46,XX,del(4)(q27q28.2)] with intact blood group-MN locus, confining its locus to 4q28.2–4q31.1 (1991)
A rapid method for starting a culture for the establishment of Epstein-Barr virus-transformed human lymphoblastoid cell lines (1992)
Detection of a cryptic paracentric inversion within band 11p13 in familial aniridia by fluorescence in situ hybridization (1993)
Microcephaly and early-onset nephrotic syndrome —confusion in Galloway-Mowat syndrome (1995)
Veröffentlichungen zu Fukushima, Yoshimitsu
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1
Fukuda, Tetsuo, Fukushima, Yoshimitsu, ... A case of an interstitial deletion of the long arm of chromosome 5: 46,XX,del(5)(q15q22)
in: Journal of human genetics , ISSN 1435-232X, Vol. 29 (1. 1984), p. 63-67
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1984
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2
Fukushima, Yoshimitsu, Niikawa, Norio, ... The Prader-Willi syndrome and interstitial deletion of chromosome 15: High-resolution chromosome analyses of 14 patients with the Prader-Willi syndrome and of 5 suspected infants
in: Journal of human genetics , ISSN 1435-232X, Vol. 29 (1. 1984), p. 1-6
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1984
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3
Fukushima, Yoshimitsu, Kuroki, Yoshikazu, ... Activity and antigen of coagulation factors VII and X in five patients with abnormal chromosome 13
in: Journal of human genetics , ISSN 1435-232X, Vol. 32 (2. 1987), p. 91-96
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1987
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4
Masuno, Mitsuo, Fukushima, Yoshimitsu, ... Partial distal 12q trisomy with arachnoid cyst
in: Journal of human genetics , ISSN 1435-232X, Vol. 32 (1. 1987), p. 39-43
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1987
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5
Fukushima, Yoshimitsu, Kuroki, Yoshikazu, ... Familial retinoblastoma (mother and son) with 13q14 deletion
in: Human genetics , ISSN 1432-1203, Vol. 77 (2. 1987), p. 104-107
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1987
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6
Masuno, Mitsuo, Fukushima, Yoshimitsu, ... Two unrelated cases of single maxillary central incisor with 7q terminal deletion
in: Journal of human genetics , ISSN 1435-232X, Vol. 35 (4. 1990), p. 311-317
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1990
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7
Yoshida, Reiko, Fukushima, Yoshimitsu, ... The Costello syndrome: Are nasal papillomata essential?
in: Journal of human genetics , ISSN 1435-232X, Vol. 38 (4. 1993), p. 437-444
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1993
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8
Ikegawa, Shiro, Fukushima, Yoshimitsu, ... Mutations of the fibroblast growth factor receptor-3 gene in one familial and six sporadic cases of achondroplasia in Japanese patients
in: Human genetics , ISSN 1432-1203, Vol. 96 (3. 1995), p. 309-311
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1995
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9
Namikawa, Chisato, Sozumori, Kaoru, ... Recurrence of osteogenesis imperfecta because of paternal mosaicism: Gly862→Ser substitution in a type I collagen gene (COL1A1)
in: Human genetics , ISSN 1432-1203, Vol. 95 (6. 1995), p. 666-670
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1995
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10
Nakajima, Hiroshi, Akasaka, Tadayoshi, ... False aneurysm of the popliteal artery treated successfully by surgery: Report of two cases
in: Surgery today , ISSN 1436-2813, Vol. 27 (9. 1997), p. 868-870
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1997
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11
Fukushima, Yoshimitsu, Fukuda, Tetsuo, ... Predisposition to autoimmune thyroiditis in ring chromosome 18 syndrome
in: Journal of human genetics , ISSN 1435-232X, Vol. 29 (2. 1984), p. 127-132
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1984
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12
Wakui, Keiko, Nishida, Toshiro, ... De novo interstitial deletion of 4q[46,XX,del(4)(q27q28.2)] with intact blood group-MN locus, confining its locus to 4q28.2–4q31.1
in: Journal of human genetics , ISSN 1435-232X, Vol. 36 (2. 1991), p. 149-153
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1991
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13
Fukushima, Yoshimitsu, Ohashi, Hirofumi, ... A rapid method for starting a culture for the establishment of Epstein-Barr virus-transformed human lymphoblastoid cell lines
in: Journal of human genetics , ISSN 1435-232X, Vol. 37 (2. 1992), p. 149-150
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1992
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14
Fukushima, Yoshimitsu, Hoovers, Jan, ... Detection of a cryptic paracentric inversion within band 11p13 in familial aniridia by fluorescence in situ hybridization
in: Human genetics , ISSN 1432-1203, Vol. 91 (3. 1993), p. 205-209
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1993
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15
Sano, Hitomi, Miyanoshita, Akihiko, ... Microcephaly and early-onset nephrotic syndrome —confusion in Galloway-Mowat syndrome
in: Pediatric nephrology , ISSN 1432-198X, Vol. 9 (6. 1995), p. 711-714
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1995
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16
Muroya, Koji, Ogata, Tsutomu, ... Refinement of the locus for X-linked recessive chondrodysplasia punctata
in: Human genetics , ISSN 1432-1203, Vol. 95 (5. 1995), p. 577-580
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1995
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17
Takahashi, Kazuhiro, Kido, Sachiko, ... Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: A prospective study
in: European journal of pediatrics , ISSN 1432-1076, Vol. 154 (11. 1995), p. 878-881
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1995
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18
Hasegawa, Tomonobu, Ogata, T., ... Coarctation of the aorta and renal hypoplasia in a boy with Turner/Noonan surface anomalies and a 46,XY karyotype: a clinical model for the possible impairment of a putative...
in: Human genetics , ISSN 1432-1203, Vol. 97 (5. 1996), p. 564-567
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1996
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19
Hasegawa, Tomonobu, Ogata, Tsutomu, ... Coarctation of the aorta and renal hypoplasia in a boy with Turner/Noonan surface anomalies and a 46,XY karyotype: A clinical model for the possible impairment of a putative...
in: Human genetics , ISSN 1432-1203, Vol. 97 (5. 1996), p. 564-567
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1996
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20
Kuwano, Akira, Morimoto, Yuji, ... Precise chromosomal locations of the genes for dentatorubral-pallidoluysian atrophy (DRPLA), von Willebrand factor (F8vWF) and parathyroid hormone-like hormone (PTHLH) in human...
in: Human genetics , ISSN 1432-1203, Vol. 97 (1. 1996), p. 95-98
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1996