G. Pai to Child
This is a "connection" page, showing publications G. Pai has written about Child.
Connection Strength
0.174
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Developmental delay timely identification and assessment. Indian Pediatr. 2010 May; 47(5):415-22.
Score: 0.041
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Diagnostic approach to children with birth defects. Indian J Pediatr. 2000 Nov; 67(11):819-23.
Score: 0.021
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Lovastatin therapy for X-linked adrenoleukodystrophy: clinical and biochemical observations on 12 patients. Mol Genet Metab. 2000 Apr; 69(4):312-22.
Score: 0.020
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A new X linked recessive syndrome of mental retardation and mild dysmorphism maps to Xq28. J Med Genet. 1997 Jul; 34(7):529-34.
Score: 0.017
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Alstr?m syndrome: a case misdiagnosed as Bardet-Biedl syndrome. J Pediatr Ophthalmol Strabismus. 1994 Jul-Aug; 31(4):272-4.
Score: 0.014
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Diagnostic approach to a child with mental retardation. Indian Pediatr. 1994 Jul; 31(7):879-90.
Score: 0.014
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Musculoaponeurotic fibromatosis (extraabdominal desmoid tumor) in a child with idiopathic multicentric osteolysis. Pediatr Dermatol. 1993 Mar; 10(1):49-53.
Score: 0.013
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Encephalocraniocutaneous lipomatosis and the Proteus syndrome: distinct entities with overlapping manifestations. Am J Med Genet. 1992 Jul 01; 43(4):662-8.
Score: 0.012
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Idiopathic multicentric osteolysis: report of two new cases and a review of the literature. Am J Med Genet. 1988 Apr; 29(4):929-36.
Score: 0.009
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Cognitive, adaptive, and behavioral characteristics of Williams syndrome. Am J Med Genet. 1997 Sep 19; 74(5):521-5.
Score: 0.004
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X-linked myotubular myopathy: clinical observations in ten additional cases. Am J Med Genet. 1995 Nov 06; 59(2):168-73.
Score: 0.004
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Heterozygote detection through bleomycin-induced G2 chromatid breakage in dyskeratosis congenita families. Cancer Genet Cytogenet. 1992 May; 60(1):31-4.
Score: 0.003
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Variability of expression of the orofaciodigital syndrome type I in black females: six cases. Am J Med Genet. 1991 Mar 15; 38(4):574-82.
Score: 0.003