Jewell A - Search Results

1

Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneity.

Haines JL, Short MP, Kwiatkowski DJ, Jewell A, Andermann E, Bejjani B, Yang CH, Gusella JF, Amos JA. Haines JL, et al. Among authors: jewell a. Am J Hum Genet. 1991 Oct;49(4):764-72. Am J Hum Genet. 1991. PMID: 1897523 Free PMC article.

2

Equal parental origin of chromosome 22 losses in human sporadic meningioma: no evidence for genomic imprinting.

Fontaine B, Rouleau GA, Seizinger B, Jewell AF, Hanson MP, Martuza RL, Gusella JF. Fontaine B, et al. Among authors: jewell af. Am J Hum Genet. 1990 Nov;47(5):823-7. Am J Hum Genet. 1990. PMID: 2220822 Free PMC article.

3

Linkage analysis in juvenile neuronal ceroid lipofuscinosis.

Haines JL, Yan WL, Boustany RM, Jewell A, Julier C, Breakefield XO, Gusella JF. Haines JL, et al. Among authors: jewell a. Am J Med Genet. 1992 Feb 15;42(4):542-5. doi: 10.1002/ajmg.1320420424. Am J Med Genet. 1992. PMID: 1609835

4

Clinical findings and linkage studies in familial tuberous sclerosis.

Short MP, Haines J, Jewell A, Bejjani B, Yang CH, Wyandt H, MacFarlane H, Andermann E, Kwiatkowski D, Amos J. Short MP, et al. Among authors: jewell a. Ann N Y Acad Sci. 1991;615:380-1. doi: 10.1111/j.1749-6632.1991.tb37788.x. Ann N Y Acad Sci. 1991. PMID: 1645505 No abstract available.

5

Molecular genetics of neurofibromatosis 2 and related tumors (acoustic neuroma and meningioma).

Fontaine B, Rouleau GA, Seizinger BR, Menon AG, Jewell AF, Martuza RL, Gusella JF. Fontaine B, et al. Among authors: jewell af. Ann N Y Acad Sci. 1991;615:338-43. doi: 10.1111/j.1749-6632.1991.tb37776.x. Ann N Y Acad Sci. 1991. PMID: 2039155 Review.

6

Parental origin of chromosome 22 loss in sporadic and NF2 neuromas.

Fontaine B, Sanson M, Delattre O, Menon AG, Rouleau GA, Seizinger BR, Jewell AF, Hanson MP, Aurias A, Martuza RL, et al. Fontaine B, et al. Among authors: jewell af. Genomics. 1991 May;10(1):280-3. doi: 10.1016/0888-7543(91)90513-e. Genomics. 1991. PMID: 1675196

7

Lethal osteosclerotic osteochondrodysplasia with platyspondyly, metaphyseal widening, and intracellular inclusions in sibs.

Brodie SG, Lachman RS, Jewell AF, Winkler CL, Nolasco L, Wilcox WR. Brodie SG, et al. Among authors: jewell af. Am J Med Genet. 1998 Dec 4;80(4):423-8. doi: 10.1002/(sici)1096-8628(19981204)80:4<423::aid-ajmg23>3.0.co;2-n. Am J Med Genet. 1998. PMID: 9856576

8

Down syndrome and comorbid autism-spectrum disorder: characterization using the aberrant behavior checklist.

Capone GT, Grados MA, Kaufmann WE, Bernad-Ripoll S, Jewell A. Capone GT, et al. Among authors: jewell a. Am J Med Genet A. 2005 May 1;134(4):373-80. doi: 10.1002/ajmg.a.30622. Am J Med Genet A. 2005. PMID: 15759262

9

Increased amyloid beta protein levels in children and adolescents with Down syndrome.

Mehta PD, Capone G, Jewell A, Freedland RL. Mehta PD, et al. Among authors: jewell a. J Neurol Sci. 2007 Mar 15;254(1-2):22-7. doi: 10.1016/j.jns.2006.12.010. Epub 2007 Feb 2. J Neurol Sci. 2007. PMID: 17275850

10

Utilization and outcomes of serial cervical cancer screening in a National Breast and Cervical Cancer Early Detection Program (NBCCEDP) in a non-Medicaid expansion state.

Ratnaparkhi R, Ismail A, Krebill H, Cook I, Javellana M, Jewell A, Spoozak L, Emerson A, Ramaswamy M, Calhoun E, Mudaranthakam DP. Ratnaparkhi R, et al. Among authors: jewell a. Cancer Causes Control. 2024 Dec 16. doi: 10.1007/s10552-024-01948-3. Online ahead of print. Cancer Causes Control. 2024. PMID: 39681764

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