Niikawa N - Search Results

1

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: niikawa n. Am J Med Genet. 1991 Nov 1;41(2):225-9. doi: 10.1002/ajmg.1320410219. Am J Med Genet. 1991. PMID: 1785639

2

DNA deletion and its parental origin in Angelman syndrome patients.

Hamabe J, Kuroki Y, Imaizumi K, Sugimoto T, Fukushima Y, Yamaguchi A, Izumikawa Y, Niikawa N. Hamabe J, et al. Among authors: niikawa n. Am J Med Genet. 1991 Oct 1;41(1):64-8. doi: 10.1002/ajmg.1320410117. Am J Med Genet. 1991. PMID: 1683160

3

Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 62 patients.

Niikawa N, Kuroki Y, Kajii T, Matsuura N, Ishikiriyama S, Tonoki H, Ishikawa N, Yamada Y, Fujita M, Umemoto H, et al. Niikawa N, et al. Am J Med Genet. 1988 Nov;31(3):565-89. doi: 10.1002/ajmg.1320310312. Am J Med Genet. 1988. PMID: 3067577 Review.

4

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. Among authors: niikawa n. Am J Med Genet. 1992 Jul 15;43(5):839-43. doi: 10.1002/ajmg.1320430517. Am J Med Genet. 1992. PMID: 1642272

5

Duplication of 8p23.2: a benign cytogenetic variant?

Harada N, Takano J, Kondoh T, Ohashi H, Hasegawa T, Sugawara H, Ida T, Yoshiura K, Ohta T, Kishino T, Kajii T, Niikawa N, Matsumoto N. Harada N, et al. Among authors: niikawa n. Am J Med Genet. 2002 Aug 15;111(3):285-8. doi: 10.1002/ajmg.10584. Am J Med Genet. 2002. PMID: 12210324

6

Exclusion mapping of the Cohen syndrome gene from the Prader-Willi syndrome locus.

Kondo I, Hamabe J, Yamamoto K, Niikawa N. Kondo I, et al. Among authors: niikawa n. Clin Genet. 1990 Dec;38(6):422-6. doi: 10.1111/j.1399-0004.1990.tb03607.x. Clin Genet. 1990. PMID: 1981180

7

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: niikawa n. Am J Med Genet. 1990 Mar;35(3):314-8. doi: 10.1002/ajmg.1320350305. Am J Med Genet. 1990. PMID: 2309778

8

Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndrome.

Abe K, Kajii T, Niikawa N. Abe K, et al. Among authors: niikawa n. Hum Genet. 1989 Jul;82(4):313-6. doi: 10.1007/BF00273988. Hum Genet. 1989. PMID: 2525515

9

The origin of mosaic Down syndrome: four cases with chromosome markers.

Niikawa N, Kajii T. Niikawa N, et al. Am J Hum Genet. 1984 Jan;36(1):123-30. Am J Hum Genet. 1984. PMID: 6230008 Free PMC article.

10

The dermatoglyphic pattern of the Kabuki make-up syndrome.

Niikawa N, Kuroki Y, Kajii T. Niikawa N, et al. Clin Genet. 1982 May;21(5):315-20. doi: 10.1111/j.1399-0004.1982.tb01378.x. Clin Genet. 1982. PMID: 7116676

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

425 results

Search Page

Filters