Naritomi K - Search Results

1

Cytogenetic and molecular study of Angelman syndrome.

Imaizumi K, Takada F, Kuroki Y, Naritomi K, Hamabe J, Niikawa N. Imaizumi K, et al. Among authors: naritomi k. Am J Med Genet. 1990 Mar;35(3):314-8. doi: 10.1002/ajmg.1320350305. Am J Med Genet. 1990. PMID: 2309778

2

[Comparison of clinical symptoms and immunological findings between two groups of patients with complete remission and persisting course of juvenile rheumatoid arthritis].

Hokonohara M, Baba Y, Yoshinaga M, Naritomi K, Kawano Y, Kawakami K, Takei S. Hokonohara M, et al. Among authors: naritomi k. Ryumachi. 1984 Jun;24(3):159-65. Ryumachi. 1984. PMID: 6505879 Japanese. No abstract available.

3

Combined Goltz and Aicardi syndromes in a terminal Xp deletion: are they a contiguous gene syndrome?

Naritomi K, Izumikawa Y, Nagataki S, Fukushima Y, Wakui K, Niikawa N, Hirayama K. Naritomi K, et al. Am J Med Genet. 1992 Jul 15;43(5):839-43. doi: 10.1002/ajmg.1320430517. Am J Med Genet. 1992. PMID: 1642272

4

Diagnostic hand anomalies in Smith-Magenis syndrome: four new patients with del (17)(p11.2p11.2).

Kondo I, Matsuura S, Kuwajima K, Tokashiki M, Izumikawa Y, Naritomi K, Niikawa N, Kajii T. Kondo I, et al. Among authors: naritomi k. Am J Med Genet. 1991 Nov 1;41(2):225-9. doi: 10.1002/ajmg.1320410219. Am J Med Genet. 1991. PMID: 1785639

5

On the genetic imprinting suggested in Angelman syndrome.

Naritomi K. Naritomi K. Am J Med Genet. 1991 Jun 15;39(4):495-7. doi: 10.1002/ajmg.1320390427. Am J Med Genet. 1991. PMID: 1877632 No abstract available.

6

Replication asynchrony between homologs 15q11.2: cytogenetic evidence for genomic imprinting.

Izumikawa Y, Naritomi K, Hirayama K. Izumikawa Y, et al. Among authors: naritomi k. Hum Genet. 1991 May;87(1):1-5. doi: 10.1007/BF01213082. Hum Genet. 1991. PMID: 2037275

7

Trisomy 9q3 syndrome: a case report and review of the literature.

Naritomi K, Izumikawa Y, Goya Y, Gushiken M, Shiroma N, Hirayama K. Naritomi K, et al. Clin Genet. 1989 Apr;35(4):293-8. doi: 10.1111/j.1399-0004.1989.tb02947.x. Clin Genet. 1989. PMID: 2653675 Review.

8

Zellweger syndrome and a microdeletion of the proximal long arm of chromosome 7.

Naritomi K, Hyakuna N, Suzuki Y, Orii T, Hirayama K. Naritomi K, et al. Hum Genet. 1988 Oct;80(2):201-2. doi: 10.1007/BF00702873. Hum Genet. 1988. PMID: 3169748

9

16q21 is critical for 16q deletion syndrome.

Naritomi K, Shiroma N, Izumikawa Y, Sameshima K, Ohdo S, Hirayama K. Naritomi K, et al. Clin Genet. 1988 May;33(5):372-5. doi: 10.1111/j.1399-0004.1988.tb03464.x. Clin Genet. 1988. PMID: 3378367

10

Delineation of the da-Silva syndrome.

Naritomi K, Tohma T, Goya Y, Shiroma N, Hirayama K. Naritomi K, et al. Am J Med Genet. 1994 Feb 1;49(3):313-6. doi: 10.1002/ajmg.1320490314. Am J Med Genet. 1994. PMID: 8209892 Review.

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