McIntosh N - Search Results

1

Ebstein anomaly: report of a familial occurrence and prenatal diagnosis.

McIntosh N, Chitayat D, Bardanis M, Fouron JC. McIntosh N, et al. Am J Med Genet. 1992 Feb 1;42(3):307-9. doi: 10.1002/ajmg.1320420309. Am J Med Genet. 1992. PMID: 1536167

2

Pulmonary atresia with intact ventricular septum and hypoplastic right heart in sibs: a single gene disorder?

Chitayat D, McIntosh N, Fouron JC. Chitayat D, et al. Among authors: mcintosh n. Am J Med Genet. 1992 Feb 1;42(3):304-6. doi: 10.1002/ajmg.1320420308. Am J Med Genet. 1992. PMID: 1536166

3

Unilateral radio-ulnar synostosis, generalized hypotonia, developmental retardation, and a characteristic facial appearance in sibs: a new syndrome.

Der Kaloustian VM, McIntosh N, Silver K, Blaichman S, Halal F. Der Kaloustian VM, et al. Among authors: mcintosh n. Am J Med Genet. 1992 Aug 1;43(6):942-5. doi: 10.1002/ajmg.1320430607. Am J Med Genet. 1992. PMID: 1384331

4

Costello syndrome.

Der Kaloustian VM, Moroz B, McIntosh N, Watters AK, Blaichman S. Der Kaloustian VM, et al. Among authors: mcintosh n. Am J Med Genet. 1991 Oct 1;41(1):69-73. doi: 10.1002/ajmg.1320410118. Am J Med Genet. 1991. PMID: 1951465

5

Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL family.

Al-Baradie R, Yamada K, St Hilaire C, Chan WM, Andrews C, McIntosh N, Nakano M, Martonyi EJ, Raymond WR, Okumura S, Okihiro MM, Engle EC. Al-Baradie R, et al. Among authors: mcintosh n. Am J Hum Genet. 2002 Nov;71(5):1195-9. doi: 10.1086/343821. Epub 2002 Oct 22. Am J Hum Genet. 2002. PMID: 12395297 Free PMC article.

6

Familial unilateral Brown syndrome.

Iannaccone A, McIntosh N, Ciccarelli ML, Baldi A, Mutolo PA, Tedesco SA, Engle EC. Iannaccone A, et al. Among authors: mcintosh n. Ophthalmic Genet. 2002 Sep;23(3):175-84. doi: 10.1076/opge.23.3.175.7882. Ophthalmic Genet. 2002. PMID: 12324876

7

CFEOM1, the classic familial form of congenital fibrosis of the extraocular muscles, is genetically heterogeneous but does not result from mutations in ARIX.

Engle EC, McIntosh N, Yamada K, Lee BA, Johnson R, O'Keefe M, Letson R, London A, Ballard E, Ruttum M, Matsumoto N, Saito N, Collins ML, Morris L, Del Monte M, Magli A, de Berardinis T. Engle EC, et al. Among authors: mcintosh n. BMC Genet. 2002;3:3. doi: 10.1186/1471-2156-3-3. Epub 2002 Mar 6. BMC Genet. 2002. PMID: 11882252 Free PMC article.

8

Genetic Counseling for Fragile X Syndrome: Recommendations of the National Society of Genetic Counselors.

McIntosh N, Gane LW, McConkie-Rosell A, Bennett RL. McIntosh N, et al. J Genet Couns. 2000 Aug;9(4):303-25. doi: 10.1023/A:1009454112907. J Genet Couns. 2000. PMID: 26141473

9

Building ICU artifact detection models with more data in less time.

Tsien CL, Kohane IS, McIntosh N. Tsien CL, et al. Among authors: mcintosh n. Proc AMIA Symp. 2001:706-10. Proc AMIA Symp. 2001. PMID: 11825277 Free PMC article.

10

Artifact detection in the PO2 and PCO2 time series monitoring data from preterm infants.

Cao C, McIntosh N, Kohane IS, Wang K. Cao C, et al. Among authors: mcintosh n. J Clin Monit Comput. 1999 Aug;15(6):369-78. doi: 10.1023/a:1009942832137. J Clin Monit Comput. 1999. PMID: 12578032

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

333 results

Search Page

Filters