Baldini A - Search Results

1

Schizophrenia and chromosomal deletions within 22q11.2.

Lindsay EA, Morris MA, Gos A, Nestadt G, Wolyniec PS, Lasseter VK, Shprintzen R, Antonarakis SE, Baldini A, Pulver AE. Lindsay EA, et al. Among authors: baldini a. Am J Hum Genet. 1995 Jun;56(6):1502-3. Am J Hum Genet. 1995. PMID: 7762575 Free PMC article. No abstract available.

2

Submicroscopic deletions at 22q11.2: variability of the clinical picture and delineation of a commonly deleted region.

Lindsay EA, Greenberg F, Shaffer LG, Shapira SK, Scambler PJ, Baldini A. Lindsay EA, et al. Among authors: baldini a. Am J Med Genet. 1995 Mar 27;56(2):191-7. doi: 10.1002/ajmg.1320560216. Am J Med Genet. 1995. PMID: 7625444

3

Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions.

Lindsay EA, Goldberg R, Jurecic V, Morrow B, Carlson C, Kucherlapati RS, Shprintzen RJ, Baldini A. Lindsay EA, et al. Among authors: baldini a. Am J Med Genet. 1995 Jul 3;57(3):514-22. doi: 10.1002/ajmg.1320570339. Am J Med Genet. 1995. PMID: 7677167

4

De novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic, and molecular characterization.

Lindsay EA, Shaffer LG, Carrozzo R, Greenberg F, Baldini A. Lindsay EA, et al. Among authors: baldini a. Am J Med Genet. 1995 Apr 10;56(3):296-9. doi: 10.1002/ajmg.1320560316. Am J Med Genet. 1995. PMID: 7778594

5

Deletion of chromosome 22q11 and pseudohypoparathyroidism.

Craigen WJ, Lindsay EA, Bricker JT, Hawkins EP, Baldini A. Craigen WJ, et al. Among authors: baldini a. Am J Med Genet. 1997 Oct 3;72(1):63-5. Am J Med Genet. 1997. PMID: 9295077

6

Congenital heart defects and 22q11 deletions: which genes count?

Lindsay EA, Baldini A. Lindsay EA, et al. Among authors: baldini a. Mol Med Today. 1998 Aug;4(8):350-7. doi: 10.1016/s1357-4310(98)01302-1. Mol Med Today. 1998. PMID: 9755454 Review.

7

Recovery from arterial growth delay reduces penetrance of cardiovascular defects in mice deleted for the DiGeorge syndrome region.

Lindsay EA, Baldini A. Lindsay EA, et al. Among authors: baldini a. Hum Mol Genet. 2001 Apr 15;10(9):997-1002. doi: 10.1093/hmg/10.9.997. Hum Mol Genet. 2001. PMID: 11309372

8

Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome.

Prescott K, Ivins S, Hubank M, Lindsay E, Baldini A, Scambler P. Prescott K, et al. Among authors: baldini a. Hum Genet. 2005 May;116(6):486-96. doi: 10.1007/s00439-005-1274-3. Epub 2005 Mar 19. Hum Genet. 2005. PMID: 15778864

9

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease.

Halford S, Wadey R, Roberts C, Daw SC, Whiting JA, O'Donnell H, Dunham I, Bentley D, Lindsay E, Baldini A, et al. Halford S, et al. Among authors: baldini a. Hum Mol Genet. 1993 Dec;2(12):2099-107. doi: 10.1093/hmg/2.12.2099. Hum Mol Genet. 1993. PMID: 8111380

10

Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 22q11.

Halford S, Lindsay E, Nayudu M, Carey AH, Baldini A, Scambler PJ. Halford S, et al. Among authors: baldini a. Hum Mol Genet. 1993 Feb;2(2):191-6. doi: 10.1093/hmg/2.2.191. Hum Mol Genet. 1993. PMID: 8499906

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