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