C I Scott
Overview
Explore the profile of C I Scott including associated specialties, affiliations and a list of published articles.
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Articles
41
Citations
295
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Recent Articles
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2.
Hoover-Fong J, McGready J, Schulze K, Barnes H, Scott C
Am J Med Genet A
. 2007 Sep;
143A(19):2227-35.
PMID: 17764078
To develop accurate weight for age charts for individuals with achondroplasia. These novel weight for age, gender-specific growth curves for achondroplasia patients from birth through 16 years were constructed from...
3.
Scott C, Iorgulescu D, Thorne H, Henderson M, Phillips K
Clin Genet
. 2003 Jul;
64(2):111-21.
PMID: 12859406
Prophylactic mastectomy (PM) is a risk-management option for women at high familial risk of breast cancer (BC). This study describes the PM experience of women enrolled in a large observational...
4.
Hong J, Barber M, Scott C, Guttenberg M, Wolfson P
J Pediatr Surg
. 1995 Dec;
30(12):1735-7.
PMID: 8749940
The authors report the case of bilateral gonadoblastomas in a phenotypic female, with a 46,XY karyotype, with campomelic dysplasia. Although campomelic dysplasia with gonadal dysgenesis should be expected to contribute...
5.
Juyal R, Finucane B, Shaffer L, Lupski J, GREENBERG F, Scott C, et al.
Am J Med Genet
. 1995 Nov;
59(3):406-7.
PMID: 8599375
No abstract available.
6.
Deere M, Blanton S, Scott C, LANGER L, Pauli R, Hecht J
Am J Hum Genet
. 1995 Mar;
56(3):698-704.
PMID: 7887425
Multiple epiphyseal dysplasia (MED) comprises a group of hereditary chondrodysplasias in which there are major anatomic abnormalities of the long tubular bones. The Fairbank and Ribbing types are the most...
7.
Sulisalo T, van der Burgt I, Rimoin D, Bonaventure J, Sillence D, Campbell J, et al.
Hum Genet
. 1995 Feb;
95(2):157-60.
PMID: 7860061
Cartilage-hair hypoplasia (CHH) is an autosomal recessive metaphyseal chondrodysplasia characterized by short stature and hypoplasia of the hair. Associated pleiotropic features include deficient erythrogenesis, impaired T-cell mediated immunity, Hirschsprung's disease,...
8.
Ihnat D, Conard K, Scott C, Singsen B
J Rheumatol
. 1993 Apr;
20(4):742-6.
PMID: 8496877
There are few observations of inflammatory synovitis in association with specific chromosomal abnormalities in children or adults. We review the genetic and rheumatic disease literature and describe the clinical, radiologic...
9.
Mandell G, Harcke H, Scott C, Caro P, Einsig H, Bowen J
Neurosurgery
. 1992 Apr;
30(4):552-6.
PMID: 1584354
Protrusio acetabuli (PA) in neurofibromatosis is not well documented in the literature. Two forms of PA, a nondysplastic and dysplastic type, are noted. Twenty-one percent of hips (13 patients) in...
10.
Grass F, McCombs J, Scott C, Young R, Moore C
Am J Med Genet
. 1984 Nov;
19(3):553-60.
PMID: 6239546
We present two children--one, 47,XY, + mar, and the other, 47,XY, + 21. Both fathers were found to have a 47,XYY chromosome constitution. The initial assumption was that the fathers'...