Lindor NM - Search Results

1

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

2

A genetic review of complete and partial hydatidiform moles and nonmolar triploidy.

Lindor NM, Ney JA, Gaffey TA, Jenkins RB, Thibodeau SN, Dewald GW. Lindor NM, et al. Mayo Clin Proc. 1992 Aug;67(8):791-9. doi: 10.1016/s0025-6196(12)60805-2. Mayo Clin Proc. 1992. PMID: 1434919 Review.

3

Central pontine myelinolysis as a complication of partial ornithine carbamoyl transferase deficiency.

Mattson LR, Lindor NM, Goldman DH, Goodwin JT, Groover RV, Vockley J. Mattson LR, et al. Among authors: lindor nm. Am J Med Genet. 1995 Jun 19;60(3):210-3. doi: 10.1002/ajmg.1320600308. Am J Med Genet. 1995. PMID: 7573173

4

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

5

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.

6

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.

7

Sanfilippo syndrome type A in two adult sibs.

Lindor NM, Hoffman A, O'Brien JF, Hanson NP, Thompson JN. Lindor NM, et al. Am J Med Genet. 1994 Nov 15;53(3):241-4. doi: 10.1002/ajmg.1320530308. Am J Med Genet. 1994. PMID: 7856659

8

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

9

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

10

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

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