Lindor NM - Search Results

1

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.

Ensenauer RE, Adeyinka A, Flynn HC, Michels VV, Lindor NM, Dawson DB, Thorland EC, Lorentz CP, Goldstein JL, McDonald MT, Smith WE, Simon-Fayard E, Alexander AA, Kulharya AS, Ketterling RP, Clark RD, Jalal SM. Ensenauer RE, et al. Among authors: lindor nm. Am J Hum Genet. 2003 Nov;73(5):1027-40. doi: 10.1086/378818. Epub 2003 Oct 2. Am J Hum Genet. 2003. PMID: 14526392 Free PMC article.

2

Xp22.3 microdeletion syndrome with microphthalmia, sclerocornea, linear skin defects, and congenital heart defects.

Lindor NM, Michels VV, Hoppe DA, Driscoll DJ, Leavitt JA, Dewald GW. Lindor NM, et al. Am J Med Genet. 1992 Sep 1;44(1):61-5. doi: 10.1002/ajmg.1320440115. Am J Med Genet. 1992. PMID: 1519653

3

Trisomy 9 mosaicism in a child with a tethered cord.

Lindor NM, Michels VV, Jalal S, Shaughnessy W. Lindor NM, et al. Clin Dysmorphol. 1995 Apr;4(2):169-72. Clin Dysmorphol. 1995. PMID: 7606325

4

Form of 15q proximal duplication appears to be a normal euchromatic variant.

Jalal SM, Persons DL, Dewald GW, Lindor NM. Jalal SM, et al. Among authors: lindor nm. Am J Med Genet. 1994 Oct 1;52(4):495-7. doi: 10.1002/ajmg.1320520421. Am J Med Genet. 1994. PMID: 7747767 No abstract available.

5

Asplenia in two father-son pairs.

Lindor NM, Smithson WA, Ahumada CA, Michels VV, Opitz JM. Lindor NM, et al. Am J Med Genet. 1995 Mar 13;56(1):10-1. doi: 10.1002/ajmg.1320560104. Am J Med Genet. 1995. PMID: 7747770 Review.

6

Screening the dystrophin gene suggests a high rate of polymorphism in general but no exonic deletions in schizophrenics.

Lindor NM, Sobell JL, Heston LL, Thibodeau SN, Sommer SS. Lindor NM, et al. Am J Med Genet. 1994 Mar 15;54(1):1-4. doi: 10.1002/ajmg.1320540102. Am J Med Genet. 1994. PMID: 7909988

7

Mosaic trisomy 16 in a thriving infant: maternal heterodisomy for chromosome 16.

Lindor NM, Jalal SM, Thibodeau SN, Bonde D, Sauser KL, Karnes PS. Lindor NM, et al. Clin Genet. 1993 Oct;44(4):185-9. doi: 10.1111/j.1399-0004.1993.tb03876.x. Clin Genet. 1993. PMID: 8261647

8

Absence of chromosome fragility at 19q13.3 in patients with myotonic dystrophy.

Jalal SM, Lindor NM, Michels VV, Buckley DD, Hoppe DA, Sarkar G, Dewald GW. Jalal SM, et al. Among authors: lindor nm. Am J Med Genet. 1993 Jun 1;46(4):441-3. doi: 10.1002/ajmg.1320460419. Am J Med Genet. 1993. PMID: 8357018

9

Autosomal dominant supravalvular aortic stenosis: localization to chromosome 7.

Olson TM, Michels VV, Lindor NM, Pastores GM, Weber JL, Schaid DJ, Driscoll DJ, Feldt RH, Thibodeau SN. Olson TM, et al. Among authors: lindor nm. Hum Mol Genet. 1993 Jul;2(7):869-73. doi: 10.1093/hmg/2.7.869. Hum Mol Genet. 1993. PMID: 8364568

10

Uniparental disomy in congenital disorders: a prospective study.

Lindor NM, Karnes PS, Michels VV, Dewald GW, Goerss J, Jalal S, Jenkins RB, Vockley G, Thibodeau SN. Lindor NM, et al. Am J Med Genet. 1995 Aug 28;58(2):143-6. doi: 10.1002/ajmg.1320580210. Am J Med Genet. 1995. PMID: 8533805

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