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Yoshimitsu Fukushima

Veröffentlichungen von Yoshimitsu Fukushima zu Yoshimitsu, Yutaka ->
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 Yoshimitsu, Yutaka
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1
Abe, Shintaro, Okubo, Yoshimitsu, ... Focal therapeutic efficacy of transcatheter arterial infusion of styrene maleic acid neocarzinostatin for hepatocellular carcinoma
in: Journal of gastroenterology , ISSN 1435-5922, Vol. 35 (1. 2000), p. 28-33
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2000
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2
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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3
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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4
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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5
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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6
Kajimoto, Y., Ryuzo, K., ... Identification of amino-acid polymorphism within the leucine zipper motif of mouse transcription factor A1
in: Gene, in: Gene . - Amsterdam : Elsevier, ISSN 0378-1119, ZDB-ID 1491012-3 Vol. 139, No. 2 (1994), p. 247-249
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1994
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7
Kimura, Hironobu, Yonemura, Yutaka, ... Prognostic factors in primary gastrointestinal leiomyosarcoma: A retrospective study
in: World journal of surgery , ISSN 1432-2323, Vol. 15 (6. 1991), p. 771-776
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1991
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8
Numabe, Hironao, Nagafuchi, Shigeo, ... DNA analyses of XX and XX-hypospadiac males
in: Human genetics , ISSN 1432-1203, Vol. 90 (3. 1992), p. 211-214
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1992
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9
Miyazaki, Kohji, Tsutsumi, Nobuo, ... 5th Japanese Association of Hepato-Biliary-Pancreatic Surgery
in: Journal of hepato-biliary-pancreatic surgery , ISSN 1436-0691, Vol. 1 (1. 1993), p. 42-104
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1993