Baldini A - Search Results

1

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

2

Chromosomal assignment of human YAC clones by fluorescence in situ hybridization: use of single-yeast-colony PCR and multiple labeling.

Baldini A, Ross M, Nizetic D, Vatcheva R, Lindsay EA, Lehrach H, Siniscalco M. Baldini A, et al. Genomics. 1992 Sep;14(1):181-4. doi: 10.1016/s0888-7543(05)80303-9. Genomics. 1992. PMID: 1427825

3

Multiple variants in subtelomeric regions of normal karyotypes.

Ijdo JW, Lindsay EA, Wells RA, Baldini A. Ijdo JW, et al. Among authors: baldini a. Genomics. 1992 Dec;14(4):1019-25. doi: 10.1016/s0888-7543(05)80125-9. Genomics. 1992. PMID: 1478643

4

Isolation and comparative mapping of a human chromosome 20-specific alpha-satellite DNA clone.

Baldini A, Archidiacono N, Carbone R, Bolino A, Shridhar V, Miller OJ, Miller DA, Ward DC, Rocchi M. Baldini A, et al. Cytogenet Cell Genet. 1992;59(1):12-6. doi: 10.1159/000133188. Cytogenet Cell Genet. 1992. PMID: 1733665

5

Rapid molecular cytogenetic analysis of X-chromosomal microdeletions: fluorescence in situ hybridization (FISH) for complex glycerol kinase deficiency.

Worley KC, Lindsay EA, Bailey W, Wise J, McCabe ER, Baldini A. Worley KC, et al. Among authors: baldini a. Am J Med Genet. 1995 Jul 17;57(4):615-9. doi: 10.1002/ajmg.1320570420. Am J Med Genet. 1995. PMID: 7573140

6

Mapping segmental imbalances using comparative genomic hybridization and eigenanalysis.

Haddad B, Antonacci R, Rizzu P, Lindsay EA, Hughes MR, Smith LC, Knapp RD, Baldini A. Haddad B, et al. Among authors: baldini a. Cytogenet Cell Genet. 1995;71(3):276-9. doi: 10.1159/000134126. Cytogenet Cell Genet. 1995. PMID: 7587393

7

Diagnosis of X-linked adrenal hypoplasia congenita by mutation analysis of the DAX1 gene.

Guo W, Mason JS, Stone CG Jr, Morgan SA, Madu SI, Baldini A, Lindsay EA, Biesecker LG, Copeland KC, Horlick MN, et al. Guo W, et al. Among authors: baldini a. JAMA. 1995 Jul 26;274(4):324-30. JAMA. 1995. PMID: 7609262

8

The gene for a human microfibril-associated glycoprotein is commonly deleted in Smith-Magenis syndrome patients.

Zhao Z, Lee CC, Jiralerspong S, Juyal RC, Lu F, Baldini A, Greenberg F, Caskey CT, Patel PI. Zhao Z, et al. Among authors: baldini a. Hum Mol Genet. 1995 Apr;4(4):589-97. doi: 10.1093/hmg/4.4.589. Hum Mol Genet. 1995. PMID: 7633408

9

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

10

Duplication 3q syndrome: molecular delineation of the critical region.

Aqua MS, Rizzu P, Lindsay EA, Shaffer LG, Zackai EH, Overhauser J, Baldini A. Aqua MS, et al. Among authors: baldini a. Am J Med Genet. 1995 Jan 2;55(1):33-7. doi: 10.1002/ajmg.1320550111. Am J Med Genet. 1995. PMID: 7702094

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