Driscoll DA - Search Results

1

Early ultrasound diagnosis of Neu-Laxova syndrome.

Rode ME, Mennuti MT, Giardine RM, Zackai EH, Driscoll DA. Rode ME, et al. Among authors: driscoll da. Prenat Diagn. 2001 Jul;21(7):575-80. doi: 10.1002/pd.101. Prenat Diagn. 2001. PMID: 11494295 Review.

2

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.

Driscoll DA, Salvin J, Sellinger B, Budarf ML, McDonald-McGinn DM, Zackai EH, Emanuel BS. Driscoll DA, et al. J Med Genet. 1993 Oct;30(10):813-7. doi: 10.1136/jmg.30.10.813. J Med Genet. 1993. PMID: 8230155 Free PMC article.

3

Omodysplasia: an affected mother and son.

Venditti CP, Farmer J, Russell KL, Friedrich CA, Alter C, Canning D, Whitaker L, Mennuti MT, Driscoll DA, Zackai EH. Venditti CP, et al. Among authors: driscoll da. Am J Med Genet. 2002 Aug 1;111(2):169-77. doi: 10.1002/ajmg.10555. Am J Med Genet. 2002. PMID: 12210345 Review.

4

Screening for Down's syndrome--too many choices?

Mennuti MT, Driscoll DA. Mennuti MT, et al. Among authors: driscoll da. N Engl J Med. 2003 Oct 9;349(15):1471-3. doi: 10.1056/NEJMe038135. N Engl J Med. 2003. PMID: 14534341 No abstract available.

5

Growth hormone deficiency in patients with 22q11.2 deletion: expanding the phenotype.

Weinzimer SA, McDonald-McGinn DM, Driscoll DA, Emanuel BS, Zackai EH, Moshang T Jr. Weinzimer SA, et al. Among authors: driscoll da. Pediatrics. 1998 May;101(5):929-32. doi: 10.1542/peds.101.5.929. Pediatrics. 1998. PMID: 9565428

6

Screening for aneuploidy in twin pregnancies: maternal age- and race-specific risk assessment between 9-14 weeks.

Odibo AO, Elkousy MH, Ural SH, Driscoll DA, Mennuti MT, Macones GA. Odibo AO, et al. Among authors: driscoll da. Twin Res. 2003 Aug;6(4):251-6. doi: 10.1375/136905203322296566. Twin Res. 2003. PMID: 14511427

7

Cerebellar atrophy in a patient with velocardiofacial syndrome.

Lynch DR, McDonald-McGinn DM, Zackai EH, Emanuel BS, Driscoll DA, Whitaker LA, Fischbeck KH. Lynch DR, et al. Among authors: driscoll da. J Med Genet. 1995 Jul;32(7):561-3. doi: 10.1136/jmg.32.7.561. J Med Genet. 1995. PMID: 7562973 Free PMC article.

8

Classical Noonan syndrome is not associated with deletions of 22q11.

Robin NH, Sellinger B, McDonald-McGinn D, Zackai EH, Emanuel BS, Driscoll DA. Robin NH, et al. Among authors: driscoll da. Am J Med Genet. 1995 Mar 13;56(1):94-6. doi: 10.1002/ajmg.1320560121. Am J Med Genet. 1995. PMID: 7747795

9

Nasal dimple as part of the 22q11.2 deletion syndrome.

Gripp KW, McDonald-McGinn DM, Driscoll DA, Reed LA, Emanuel BS, Zackai EH. Gripp KW, et al. Among authors: driscoll da. Am J Med Genet. 1997 Mar 31;69(3):290-2. Am J Med Genet. 1997. PMID: 9096759

10

Increased prevalence of immunoglobulin A deficiency in patients with the chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

Smith CA, Driscoll DA, Emanuel BS, McDonald-McGinn DM, Zackai EH, Sullivan KE. Smith CA, et al. Among authors: driscoll da. Clin Diagn Lab Immunol. 1998 May;5(3):415-7. doi: 10.1128/CDLI.5.3.415-417.1998. Clin Diagn Lab Immunol. 1998. PMID: 9606003 Free PMC article.

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