Pai GS - Search Results

1

Alström syndrome: a case misdiagnosed as Bardet-Biedl syndrome.

Dyer DS, Wilson ME, Small KW, Pai GS. Dyer DS, et al. Among authors: pai gs. J Pediatr Ophthalmol Strabismus. 1994 Jul-Aug;31(4):272-4. doi: 10.3928/0191-3913-19940701-19. J Pediatr Ophthalmol Strabismus. 1994. PMID: 7807310 No abstract available.

2

Diagnostic approach to a child with mental retardation.

Pai GS. Pai GS. Indian Pediatr. 1994 Jul;31(7):879-90. Indian Pediatr. 1994. PMID: 7890364 Review. No abstract available.

3

Diagnostic approach to children with birth defects.

Pai GS, Gadewar SB. Pai GS, et al. Indian J Pediatr. 2000 Nov;67(11):819-23. doi: 10.1007/BF02726226. Indian J Pediatr. 2000. PMID: 11216382 Review.

4

A new Seckel-like syndrome of primordial dwarfism.

Buebel MS, Salinas CF, Pai GS, Macpherson RI, Greer MK, Perez-Comas A. Buebel MS, et al. Among authors: pai gs. Am J Med Genet. 1996 Aug 23;64(3):447-52. doi: 10.1002/(SICI)1096-8628(19960823)64:3<447::AID-AJMG1>3.0.CO;2-M. Am J Med Genet. 1996. PMID: 8862620

5

Walker-Warburg syndrome: report of three affected sibs.

Rodgers BL, Vanner LV, Pai GS, Sens MA. Rodgers BL, et al. Among authors: pai gs. Am J Med Genet. 1994 Jan 15;49(2):198-201. doi: 10.1002/ajmg.1320490207. Am J Med Genet. 1994. PMID: 8116667

6

Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.

Leonardi ML, Pai GS, Wilkes B, Lebel RR. Leonardi ML, et al. Among authors: pai gs. Am J Med Genet. 2001 Aug 15;102(3):237-42. Am J Med Genet. 2001. PMID: 11484200 Review.

7

Musculoaponeurotic fibromatosis (extraabdominal desmoid tumor) in a child with idiopathic multicentric osteolysis.

Sahn EE, Cook WJ, Gross RH, Garen PD, Pai GS. Sahn EE, et al. Among authors: pai gs. Pediatr Dermatol. 1993 Mar;10(1):49-53. doi: 10.1111/j.1525-1470.1993.tb00014.x. Pediatr Dermatol. 1993. PMID: 8493169

8

Neurologic disease in a child with hepatoerythropoietic porphyria.

Parsons JL, Sahn EE, Holden KR, Pai GS. Parsons JL, et al. Among authors: pai gs. Pediatr Dermatol. 1994 Sep;11(3):216-21. doi: 10.1111/j.1525-1470.1994.tb00589.x. Pediatr Dermatol. 1994. PMID: 7971555

9

Autism spectrum disorder, Klinefelter syndrome, and chromosome 3p21.31 duplication: a case report.

Stuart SW, King CH, Pai GS. Stuart SW, et al. Among authors: pai gs. MedGenMed. 2007 Dec 18;9(4):60. MedGenMed. 2007. PMID: 18311409 Free PMC article.

10

A new X linked recessive syndrome of mental retardation and mild dysmorphism maps to Xq28.

Pai GS, Hane B, Joseph M, Nelson R, Hammond LS, Arena JF, Lubs HA, Stevenson RE, Schwartz CE. Pai GS, et al. J Med Genet. 1997 Jul;34(7):529-34. doi: 10.1136/jmg.34.7.529. J Med Genet. 1997. PMID: 9222958 Free PMC article.

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