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Interstitial deletion of chromosome 18[del(18)(q11.2q12.2 or q12.2q21.1].
Surh LC, Ledbetter DH, Greenberg F. Surh LC, et al. Am J Med Genet. 1991 Oct 1;41(1):15-7. doi: 10.1002/ajmg.1320410105. Am J Med Genet. 1991. PMID: 1719812
New somatic cell hybrids for physical mapping in distal Xq and the fragile X region.
Ledbetter SA, Schwartz CE, Davies KE, Ledbetter DH. Ledbetter SA, et al. Am J Med Genet. 1991 Feb-Mar;38(2-3):418-20. doi: 10.1002/ajmg.1320380254. Am J Med Genet. 1991. PMID: 2018083
Detection of a subtle rearrangement of chromosome 22 using molecular techniques.
Biesecker LG, Rosenberg M, Dziadzio L, Ledbetter DH, Ning Y, Sarneso C, Rosenbaum K. Biesecker LG, et al. Am J Med Genet. 1995 Sep 25;58(4):389-94. doi: 10.1002/ajmg.1320580426. Am J Med Genet. 1995. PMID: 8533859 Review.
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. 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. 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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