Pagon RA - Search Results

1

Incidence of tuberous sclerosis in patients with cardiac rhabdomyoma.

Harding CO, Pagon RA. Harding CO, et al. Among authors: pagon ra. Am J Med Genet. 1990 Dec;37(4):443-6. doi: 10.1002/ajmg.1320370402. Am J Med Genet. 1990. PMID: 2260584 Review.

2

Twin fetuses with abnormalities that overlap with three midline malformation complexes.

Hingorani SR, Pagon RA, Shepard TH, Kapur RP. Hingorani SR, et al. Among authors: pagon ra. Am J Med Genet. 1991 Nov 1;41(2):230-5. doi: 10.1002/ajmg.1320410220. Am J Med Genet. 1991. PMID: 1785640

3

Mosaic isochromosome 8p.

Tilstra DJ, Grove M, Spencer AC, Norwood TH, Pagon RA. Tilstra DJ, et al. Among authors: pagon ra. Am J Med Genet. 1993 Jun 15;46(5):517-9. doi: 10.1002/ajmg.1320460511. Am J Med Genet. 1993. PMID: 8322812 Review.

4

Digital anomalies, microcephaly, and normal intelligence: new syndrome or Feingold syndrome?

Kawame H, Pagon RA, Hudgins L. Kawame H, et al. Among authors: pagon ra. Am J Med Genet. 1997 Mar 31;69(3):240-4. doi: 10.1002/(sici)1096-8628(19970331)69:3<240::aid-ajmg6>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9096751

5

Autosomal dominant inheritance of Barber-Say syndrome.

Dinulos MB, Pagon RA. Dinulos MB, et al. Among authors: pagon ra. Am J Med Genet. 1999 Sep 3;86(1):54-6. doi: 10.1002/(sici)1096-8628(19990903)86:1<54::aid-ajmg10>3.0.co;2-2. Am J Med Genet. 1999. PMID: 10440829

6

Facio-oculo-acoustico-renal (FOAR) syndrome: case report and review.

Schowalter DB, Pagon RA, Kalina RE, McDonald R. Schowalter DB, et al. Among authors: pagon ra. Am J Med Genet. 1997 Mar 3;69(1):45-9; discussion 44. doi: 10.1002/(sici)1096-8628(19970303)69:1<45::aid-ajmg9>3.0.co;2-s. Am J Med Genet. 1997. PMID: 9066882 Review.

7

Prevalence of hypopigmented macules in a healthy population.

Vanderhooft SL, Francis JS, Pagon RA, Smith LT, Sybert VP. Vanderhooft SL, et al. Among authors: pagon ra. J Pediatr. 1996 Sep;129(3):355-61. doi: 10.1016/s0022-3476(96)70066-5. J Pediatr. 1996. PMID: 8804323

8

Partial deletion of the long arm of chromosome 11 [del(11)(q23.3----qter)] with abnormal white matter.

Wardinsky TD, Weinberger E, Pagon RA, Clarren SK, Thuline HC. Wardinsky TD, et al. Among authors: pagon ra. Am J Med Genet. 1990 Jan;35(1):60-3. doi: 10.1002/ajmg.1320350111. Am J Med Genet. 1990. PMID: 2301470

9

X-linked sideroblastic anemia and ataxia: linkage to phosphoglycerate kinase at Xq13.

Raskind WH, Wijsman E, Pagon RA, Cox TC, Bawden MJ, May BK, Bird TD. Raskind WH, et al. Among authors: pagon ra. Am J Hum Genet. 1991 Feb;48(2):335-41. Am J Hum Genet. 1991. PMID: 1671320 Free PMC article.

10

Simpson-Golabi-Behmel syndrome: genotype/phenotype analysis of 18 affected males from 7 unrelated families.

Hughes-Benzie RM, Pilia G, Xuan JY, Hunter AG, Chen E, Golabi M, Hurst JA, Kobori J, Marymee K, Pagon RA, Punnett HH, Schelley S, Tolmie JL, Wohlferd MM, Grossman T, Schlessinger D, MacKenzie AE. Hughes-Benzie RM, et al. Among authors: pagon ra. Am J Med Genet. 1996 Dec 11;66(2):227-34. doi: 10.1002/(SICI)1096-8628(19961211)66:2<227::AID-AJMG20>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8958336

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