DC02027/DC/NIDCD NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1995	1
1996	4
1997	10
1998	5
1999	8
2000	5
2001	9
2002	4
2003	3
2004	3
2005	2
2006	3
2007	1
2008	2
2009	2
2024	0

1

Prenatal diagnosis of the 22q11.2 deletion syndrome.

Driscoll DA. Driscoll DA. Genet Med. 2001 Jan-Feb;3(1):14-8. doi: 10.1097/00125817-200101000-00004. Genet Med. 2001. PMID: 11339370 Free article. Review.

2

Progress in the autosomal segmental aneusomy syndromes (SASs): single or multi-locus disorders?

Budarf ML, Emanuel BS. Budarf ML, et al. Hum Mol Genet. 1997;6(10):1657-65. doi: 10.1093/hmg/6.10.1657. Hum Mol Genet. 1997. PMID: 9300657 Review.

3

Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: an update and literature review.

Shaikh TH, Kurahashi H, Emanuel BS. Shaikh TH, et al. Genet Med. 2001 Jan-Feb;3(1):6-13. doi: 10.1097/00125817-200101000-00003. Genet Med. 2001. PMID: 11339380 Free article. Review.

4

Molecular and genetic aspects of DiGeorge/velocardiofacial syndrome.

Driscoll DA. Driscoll DA. Methods Mol Med. 2006;126:43-55. doi: 10.1385/1-59745-088-X:43. Methods Mol Med. 2006. PMID: 16930005

5

Research on behavioral phenotypes: velocardiofacial syndrome (deletion 22q11.2).

Wang PP, Woodin MF, Kreps-Falk R, Moss EM. Wang PP, et al. Dev Med Child Neurol. 2000 Jun;42(6):422-7. doi: 10.1017/s0012162200000785. Dev Med Child Neurol. 2000. PMID: 10875531 Free article. Review. No abstract available.

6

Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion.

Woodin M, Wang PP, Aleman D, McDonald-McGinn D, Zackai E, Moss E. Woodin M, et al. Genet Med. 2001 Jan-Feb;3(1):34-9. doi: 10.1097/00125817-200101000-00008. Genet Med. 2001. PMID: 11339375 Free article.

7

Taking advantage of early diagnosis: preschool children with the 22q11.2 deletion.

Gerdes M, Solot C, Wang PP, McDonald-McGinn DM, Zackai EH. Gerdes M, et al. Genet Med. 2001 Jan-Feb;3(1):40-4. doi: 10.1097/00125817-200101000-00009. Genet Med. 2001. PMID: 11339376 Free article.

8

The Philadelphia story: the 22q11.2 deletion: report on 250 patients.

McDonald-McGinn DM, Kirschner R, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Solot C, Wang P, Jacobs I, Handler S, Knightly C, Heher K, Wilson M, Ming JE, Grace K, Driscoll D, Pasquariello P, Randall P, Larossa D, Emanuel BS, Zackai EH. McDonald-McGinn DM, et al. Genet Couns. 1999;10(1):11-24. Genet Couns. 1999. PMID: 10191425

9

Communication issues in 22q11.2 deletion syndrome: children at risk.

Solot CB, Gerdes M, Kirschner RE, McDonald-McGinn DM, Moss E, Woodin M, Aleman D, Zackai EH, Wang PP. Solot CB, et al. Genet Med. 2001 Jan-Feb;3(1):67-71. doi: 10.1097/00125817-200101000-00015. Genet Med. 2001. PMID: 11339383 Free article.

10

Chromosomal and cardiovascular anomalies associated with congenital laryngeal web.

McElhinney DB, Jacobs I, McDonald-McGinn DM, Zackai EH, Goldmuntz E. McElhinney DB, et al. Int J Pediatr Otorhinolaryngol. 2002 Oct 21;66(1):23-27. doi: 10.1016/s0165-5876(02)00184-2. Int J Pediatr Otorhinolaryngol. 2002. PMID: 12363418

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