G. Pai to Female
This is a "connection" page, showing publications G. Pai has written about Female.
Connection Strength
0.123
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Developmental delay timely identification and assessment. Indian Pediatr. 2010 May; 47(5):415-22.
Score: 0.019
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Atypical aplasia cutis in association with Xia Gibbs syndrome. Pediatr Dermatol. 2021 Mar; 38(2):533-535.
Score: 0.010
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Diagnostic approach to children with birth defects. Indian J Pediatr. 2000 Nov; 67(11):819-23.
Score: 0.010
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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: 0.009
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Mosaic trisomy 8: a cautionary note regarding missed antenatal diagnosis. J Perinatol. 1998 Jan-Feb; 18(1):78-80.
Score: 0.008
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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: 0.008
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An atypical Turner syndrome patient with ring X chromosome mosaicism. Ann Clin Lab Sci. 1995 Jan-Feb; 25(1):60-5.
Score: 0.007
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Neurologic disease in a child with hepatoerythropoietic porphyria. Pediatr Dermatol. 1994 Sep; 11(3):216-21.
Score: 0.006
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Diagnostic approach to a child with mental retardation. Indian Pediatr. 1994 Jul; 31(7):879-90.
Score: 0.006
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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: 0.006
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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: 0.006
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Bleomycin hypersensitivity in dyskeratosis congenita fibroblasts, lymphocytes, and transformed lymphoblasts. Cytogenet Cell Genet. 1989; 52(3-4):186-9.
Score: 0.004
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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: 0.004
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Mosaic duplication 1(q11q44) in an infant with nephroblastomatosis and mineralization of extraplacental membranes. Pediatr Dev Pathol. 2005 Jan-Feb; 8(1):115-23.
Score: 0.003
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Cognitive, adaptive, and behavioral characteristics of Williams syndrome. Am J Med Genet. 1997 Sep 19; 74(5):521-5.
Score: 0.002
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Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocation. J Med Genet. 1996 Nov; 33(11):906-11.
Score: 0.002
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A new Seckel-like syndrome of primordial dwarfism. Am J Med Genet. 1996 Aug 23; 64(3):447-52.
Score: 0.002
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Mosaic vs. nonmosaic trisomy 9: report of a liveborn infant evaluated by fluorescence in situ hybridization and review of the literature. Am J Med Genet. 1996 Apr 24; 62(4):330-5.
Score: 0.002
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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: 0.002
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Molecular analysis of a complex chromosomal rearrangement and a review of familial cases. Am J Med Genet. 1994 Nov 15; 53(3):255-63.
Score: 0.002
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Walker-Warburg syndrome: report of three affected sibs. Am J Med Genet. 1994 Jan 15; 49(2):198-201.
Score: 0.002
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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: 0.001
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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: 0.001
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Enhanced G2 chromatid radiosensitivity in dyskeratosis congenita fibroblasts. Am J Hum Genet. 1990 Feb; 46(2):350-7.
Score: 0.001