Saitoh S - Search Results

1

Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis.

Kuwano A, Mutirangura A, Dittrich B, Buiting K, Horsthemke B, Saitoh S, Niikawa N, Ledbetter SA, Greenberg F, Chinault AC, et al. Kuwano A, et al. Among authors: saitoh s. Hum Mol Genet. 1992 Sep;1(6):417-25. doi: 10.1093/hmg/1.6.417. Hum Mol Genet. 1992. PMID: 1363801

2

Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor beta 3-subunit gene.

Saitoh S, Kubota T, Ohta T, Jinno Y, Niikawa N, Sugimoto T, Wagstaff J, Lalande M. Saitoh S, et al. Lancet. 1992 Feb 8;339(8789):366-7. doi: 10.1016/0140-6736(92)91686-3. Lancet. 1992. PMID: 1346439 No abstract available.

3

Angelman syndrome in three siblings: characteristic epileptic seizures and EEG abnormalities.

Sugimoto T, Yasuhara A, Ohta T, Nishida N, Saitoh S, Hamabe J, Niikawa N. Sugimoto T, et al. Among authors: saitoh s. Epilepsia. 1992 Nov-Dec;33(6):1078-82. doi: 10.1111/j.1528-1157.1992.tb01762.x. Epilepsia. 1992. PMID: 1464267

4

A BsaBI RFLP detected for probe pML34 [D15S9] on chromosome 15q.

Hamabe J, Saitoh S, Niikawa N. Hamabe J, et al. Among authors: saitoh s. Nucleic Acids Res. 1991 Sep 11;19(17):4789. doi: 10.1093/nar/19.17.4789. Nucleic Acids Res. 1991. PMID: 1679924 Free PMC article.

5

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

Buiting K, Saitoh S, Gross S, Dittrich B, Schwartz S, Nicholls RD, Horsthemke B. Buiting K, et al. Among authors: saitoh s. Nat Genet. 1995 Apr;9(4):395-400. doi: 10.1038/ng0495-395. Nat Genet. 1995. PMID: 7795645

6

Molecular and clinical study of 61 Angelman syndrome patients.

Saitoh S, Harada N, Jinno Y, Hashimoto K, Imaizumi K, Kuroki Y, Fukushima Y, Sugimoto T, Renedo M, Wagstaff J, et al. Saitoh S, et al. Am J Med Genet. 1994 Aug 15;52(2):158-63. doi: 10.1002/ajmg.1320520207. Am J Med Genet. 1994. PMID: 7802001 Review.

7

A common insertion/deletion polymorphism in the Prader-Willi syndrome minimal critical region.

Gabriel J, Gottlieb W, Garcia A, Rogan PK, Saitoh S, Nicholls RD. Gabriel J, et al. Among authors: saitoh s. Hum Mol Genet. 1994 Oct;3(10):1912. doi: 10.1093/hmg/3.10.1912. Hum Mol Genet. 1994. PMID: 7849727 No abstract available.

8

Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome.

Kubota T, Saitoh S, Matsumoto T, Narahara K, Fukushima Y, Jinno Y, Niikawa N. Kubota T, et al. Among authors: saitoh s. Am J Med Genet. 1994 Feb 15;49(4):378-83. doi: 10.1002/ajmg.1320490405. Am J Med Genet. 1994. PMID: 7909196

9

Isochromosome 15q of maternal origin in two Prader-Willi syndrome patients previously diagnosed erroneously as cytogenetic deletions.

Saitoh S, Mutirangura A, Kuwano A, Ledbetter DH, Niikawa N. Saitoh S, et al. Am J Med Genet. 1994 Mar 1;50(1):64-7. doi: 10.1002/ajmg.1320500114. Am J Med Genet. 1994. PMID: 7909198

10

Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients.

Glenn CC, Nicholls RD, Robinson WP, Saitoh S, Niikawa N, Schinzel A, Horsthemke B, Driscoll DJ. Glenn CC, et al. Among authors: saitoh s. Hum Mol Genet. 1993 Sep;2(9):1377-82. doi: 10.1093/hmg/2.9.1377. Hum Mol Genet. 1993. PMID: 8242060 Free article.

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