Kittikamron K[au] - Search Results

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Year	Number of Results
1996	1
1997	1
1998	2
1999	1
2022	0

Page 1

Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndrome.

Carrozzo R, Rossi E, Christian SL, Kittikamron K, Livieri C, Corrias A, Pucci L, Fois A, Simi P, Bosio L, Beccaria L, Zuffardi O, Ledbetter DH. Carrozzo R, et al. Among authors: kittikamron k. Am J Hum Genet. 1997 Jul;61(1):228-31. doi: 10.1086/513907. Am J Hum Genet. 1997. PMID: 9246004 Free PMC article. No abstract available.

Isolation of BAC clones spanning the Xq22.3 translocation breakpoint in a lissencephaly patient with a de novo X;2 translocation.

Matsumoto N, Pilz DT, Fantes JA, Kittikamron K, Ledbetter DH. Matsumoto N, et al. Among authors: kittikamron k. J Med Genet. 1998 Oct;35(10):829-32. doi: 10.1136/jmg.35.10.829. J Med Genet. 1998. PMID: 9783706 Free PMC article.

Two 22q telomere deletions serendipitously detected by FISH.

Precht KS, Lese CM, Spiro RP, Huttenlocher PR, Johnston KM, Baker JC, Christian SL, Kittikamron K, Ledbetter DH. Precht KS, et al. Among authors: kittikamron k. J Med Genet. 1998 Nov;35(11):939-42. doi: 10.1136/jmg.35.11.939. J Med Genet. 1998. PMID: 9832042 Free PMC article.

Preparative-scale purification of RNA using an efficient method which combines gel electrophoresis and column chromatography.

Cunningham L, Kittikamron K, Lu Y. Cunningham L, et al. Among authors: kittikamron k. Nucleic Acids Res. 1996 Sep 15;24(18):3647-8. doi: 10.1093/nar/24.18.3647. Nucleic Acids Res. 1996. PMID: 8836197 Free PMC article.

Significance of genetic testing for paternal uniparental disomy of chromosome 6 in neonatal diabetes mellitus.

Christian SL, Rich BH, Loebl C, Israel J, Vasa R, Kittikamron K, Spiro R, Rosenfield R, Ledbetter DH. Christian SL, et al. Among authors: kittikamron k. J Pediatr. 1999 Jan;134(1):42-6. doi: 10.1016/s0022-3476(99)70370-7. J Pediatr. 1999. PMID: 9880447

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