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Fetal stroke.
Ozduman K, Pober BR, Barnes P, Copel JA, Ogle EA, Duncan CC, Ment LR. Ozduman K, et al. Among authors: pober br. Pediatr Neurol. 2004 Mar;30(3):151-62. doi: 10.1016/j.pediatrneurol.2003.08.004. Pediatr Neurol. 2004. PMID: 15033196 Review.
A better understanding of those risk factors predisposing a fetus to cerebral infarction may provide a basis for future therapeutic intervention trials. Ozduman K, Pober BR, Barnes P, Copel JA, Ogle EA, Duncan CC, Ment LR. Fetal stroke....
A better understanding of those risk factors predisposing a fetus to cerebral infarction may provide a basis for future therapeutic interven …
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. Among authors: pober br. 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
Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophy.
Brown CA, Lanning RW, McKinney KQ, Salvino AR, Cherniske E, Crowe CA, Darras BT, Gominak S, Greenberg CR, Grosmann C, Heydemann P, Mendell JR, Pober BR, Sasaki T, Shapiro F, Simpson DA, Suchowersky O, Spence JE. Brown CA, et al. Among authors: pober br. Am J Med Genet. 2001 Sep 1;102(4):359-67. doi: 10.1002/ajmg.1463. Am J Med Genet. 2001. PMID: 11503164
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: pober br. Hum Mol Genet. 2001 May 15;10(11):1185-9. doi: 10.1093/hmg/10.11.1185. Hum Mol Genet. 2001. PMID: 11371511
Early puberty in Williams syndrome.
Cherniske EM, Sadler LS, Schwartz D, Carpenter TO, Pober BR. Cherniske EM, et al. Among authors: pober br. Clin Dysmorphol. 1999 Apr;8(2):117-21. Clin Dysmorphol. 1999. PMID: 10319200
111 results