Battaglia A - Search Results

1

Further characterization of the new microdeletion syndrome of 16p11.2-p12.2.

Battaglia A, Novelli A, Bernardini L, Igliozzi R, Parrini B. Battaglia A, et al. Am J Med Genet A. 2009 Jun;149A(6):1200-4. doi: 10.1002/ajmg.a.32847. Am J Med Genet A. 2009. PMID: 19449418

2

Diagnostic yield of the comprehensive assessment of developmental delay/mental retardation in an institute of child neuropsychiatry.

Battaglia A, Bianchini E, Carey JC. Battaglia A, et al. Am J Med Genet. 1999 Jan 1;82(1):60-6. Am J Med Genet. 1999. PMID: 9916845

3

"Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype.

Zollino M, Wright TJ, Di Stefano C, Tosolini A, Battaglia A, Altherr MR, Neri G. Zollino M, et al. Among authors: battaglia a. Am J Med Genet. 1999 Feb 19;82(5):371-5. Am J Med Genet. 1999. PMID: 10069706

4

Natural history of Wolf-Hirschhorn syndrome: experience with 15 cases.

Battaglia A, Carey JC, Cederholm P, Viskochil DH, Brothman AR, Galasso C. Battaglia A, et al. Pediatrics. 1999 Apr;103(4 Pt 1):830-6. doi: 10.1542/peds.103.4.830. Pediatrics. 1999. PMID: 10103318

5

Health supervision and anticipatory guidance of individuals with Wolf-Hirschhorn syndrome.

Battaglia A, Carey JC. Battaglia A, et al. Am J Med Genet. 1999 Jun 25;89(2):111-5. doi: 10.1002/(sici)1096-8628(19990625)89:2<111::aid-ajmg9>3.0.co;2-g. Am J Med Genet. 1999. PMID: 10559766 Review.

Wolf-Hirschhorn syndrome (WHS) is a well-known malformation syndrome due to microdeletion of the short arm of chromosome 4 (4p-). ...It is generally thought that these children have severe developmental disabilities and tend to be mere survivors devoid of personality. It i …

Wolf-Hirschhorn syndrome (WHS) is a well-known malformation syndrome due to microdeletion of the short arm of chromosome 4 (4p-). ... …

6

Wolf-Hirschhorn syndrome (WHS): a history in pictures.

Battaglia A, Carey JC, Viskochil DH, Cederholm P, Opitz JM. Battaglia A, et al. Clin Dysmorphol. 2000 Jan;9(1):25-30. doi: 10.1097/00019605-200009010-00005. Clin Dysmorphol. 2000. PMID: 10649793

7

del (9p) syndrome: proposed behavior phenotype.

Chilosi A, Battaglia A, Brizzolara D, Cipriani P, Pfanner L, Carey JC. Chilosi A, et al. Among authors: battaglia a. Am J Med Genet. 2001 Apr 22;100(2):138-44. doi: 10.1002/ajmg.1230. Am J Med Genet. 2001. PMID: 11298375

8

Recombinant 4 syndrome due to an unbalanced pericentric inversion of chromosome 4.

Battaglia A, Brothman AR, Carey JC. Battaglia A, et al. Am J Med Genet. 2002 Sep 15;112(1):103-6. doi: 10.1002/ajmg.10640. Am J Med Genet. 2002. PMID: 12239731

9

Diagnostic evaluation of developmental delay/mental retardation: An overview.

Battaglia A, Carey JC. Battaglia A, et al. Am J Med Genet C Semin Med Genet. 2003 Feb 15;117C(1):3-14. doi: 10.1002/ajmg.c.10015. Am J Med Genet C Semin Med Genet. 2003. PMID: 12561053 Review.

10

Neuroimaging studies in the evaluation of developmental delay/mental retardation.

Battaglia A. Battaglia A. Am J Med Genet C Semin Med Genet. 2003 Feb 15;117C(1):25-30. doi: 10.1002/ajmg.c.10017. Am J Med Genet C Semin Med Genet. 2003. PMID: 12561055 Review.

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