Lindor NM - Search Results

1

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

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

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

4

Initial assessment of infants and children with suspected inborn errors of metabolism.

Lindor NM, Karnes PS. Lindor NM, et al. Mayo Clin Proc. 1995 Oct;70(10):987-8. doi: 10.4065/70.10.987. Mayo Clin Proc. 1995. PMID: 7564553 No abstract available.

5

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

6

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

7

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.

8

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.

9

Mutations in the RET protooncogene in sporadic pheochromocytomas.

Lindor NM, Honchel R, Khosla S, Thibodeau SN. Lindor NM, et al. J Clin Endocrinol Metab. 1995 Feb;80(2):627-9. doi: 10.1210/jcem.80.2.7852530. J Clin Endocrinol Metab. 1995. PMID: 7852530

10

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

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