Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

105 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Inverted insertion of chromosome 7q and ectrodactyly.
Naritomi K, Izumikawa Y, Tohma T, Hirayama K. Naritomi K, et al. Am J Med Genet. 1993 Jun 15;46(5):492-3. doi: 10.1002/ajmg.1320460505. Am J Med Genet. 1993. PMID: 8322806
Y-derived sequence detected in minute chromosomes by polymerase chain reaction and in situ hybridization.
Tsukahara M, Matsuura S, Kishi F, Fisher LK, Stock AD, Izumikawa Y, Naritomi K, Kajii T. Tsukahara M, et al. Among authors: naritomi k. Clin Genet. 1992 Aug;42(2):80-3. doi: 10.1111/j.1399-0004.1992.tb03144.x. Clin Genet. 1992. PMID: 1424235
Pigmentary dysplasias and chromosomal mosaicism: report of 9 cases.
Ohashi H, Tsukahara M, Murano I, Naritomi K, Nishioka K, Miyake S, Kajii T. Ohashi H, et al. Among authors: naritomi k. Am J Med Genet. 1992 Jul 1;43(4):716-21. doi: 10.1002/ajmg.1320430413. Am J Med Genet. 1992. PMID: 1621763
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
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
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.
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
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
Gene assignment of Zellweger syndrome to 7q11.23: report of the second case associated with a pericentric inversion of chromosome 7.
Naritomi K, Izumikawa Y, Ohshiro S, Yoshida K, Shimozawa N, Suzuki Y, Orii T, Hirayama K. Naritomi K, et al. Hum Genet. 1989 Dec;84(1):79-80. doi: 10.1007/BF00210677. Hum Genet. 1989. PMID: 2606480
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.
105 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page
Feedback