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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1998 1
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2001 2
2004 1
2013 1
2022 0
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Page 1
Truncating mutations in FOXC2 cause multiple lymphedema syndromes.
Finegold DN, Kimak MA, Lawrence EC, Levinson KL, Cherniske EM, Pober BR, Dunlap JW, Ferrell RE. Finegold DN, et al. Among authors: cherniske em. Hum Mol Genet. 2001 May 15;10(11):1185-9. doi: 10.1093/hmg/10.11.1185. Hum Mol Genet. 2001. PMID: 11371511
Multisystem study of 20 older adults with Williams syndrome.
Cherniske EM, Carpenter TO, Klaiman C, Young E, Bregman J, Insogna K, Schultz RT, Pober BR. Cherniske EM, et al. Am J Med Genet A. 2004 Dec 15;131(3):255-64. doi: 10.1002/ajmg.a.30400. Am J Med Genet A. 2004. PMID: 15534874
Early puberty in Williams syndrome.
Cherniske EM, Sadler LS, Schwartz D, Carpenter TO, Pober BR. Cherniske EM, et al. Clin Dysmorphol. 1999 Apr;8(2):117-21. Clin Dysmorphol. 1999. PMID: 10319200