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

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

4

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.

5

Genitourinary malformations in chromosome 22q11.2 deletion.

Wu HY, Rusnack SL, Bellah RD, Plachter N, McDonald-McGinn DM, Zackai EH, Canning DA. Wu HY, et al. J Urol. 2002 Dec;168(6):2564-5. doi: 10.1016/S0022-5347(05)64215-2. J Urol. 2002. PMID: 12441983

6

Chromosome 22q11 deletion in patients with truncus arteriosus.

McElhinney DB, Driscoll DA, Emanuel BS, Goldmuntz E. McElhinney DB, et al. Pediatr Cardiol. 2003 Nov-Dec;24(6):569-73. doi: 10.1007/s00246-003-0441-3. Epub 2003 Sep 4. Pediatr Cardiol. 2003. PMID: 12947506

7

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.

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

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.

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

60 results

Results by year

Search Page

Filters

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

Search Results

60 results

Results by year