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11 . Academic Journal
Variation in IRF6 contributes to nonsyndromic cleft lip and palate
저자
by
Blanton, SH
;
Cortez, A
;
Stal, S
;
Mulliken, JB
;
Finnell, RH
, et al.
소스
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
; SEP 1 2005, 137A 3, p259-p262, 4p.
Scopus
Web of Science
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17 . Academic Journal
Confirmation of linkage and refinement of the RP28 locus for autosomal recessive retinitis pigmentosa on chromosome 2p14-p15 in an Indian family
저자
by
Kumar, A
;
Shetty, J
;
Kumar, B
;
Blanton, SH
.
소스
MOLECULAR VISION
; JUN 15 2004, 10 49-50, p399-p402, 4p.
Scopus
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16 . Academic Journal
Association of chromosomal regions 3p21.2, 10p13, and 16p13.3 with nonsyndromic cleft lip and palate
저자
by
Blanton, SH
;
Bertin, T
;
Serna, ME
;
Stal, S
;
Mulliken, JB
, et al.
소스
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
; FEB 15 2004, 125A 1, p23-p27, 5p.
Scopus
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17 . Academic Journal
Nonsyndromic cleft lip and palate: Four chromosomal regions of interest
저자
by
Blanton, SH
;
Bertin, T
;
Patel, S
;
Stal, S
;
Mulliken, JB
, et al.
소스
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
; FEB 15 2004, 125A 1, p28-p37, 10p.
Scopus
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17 . Academic Journal
Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands
저자
by
Pandya, A
;
Arnos, KS
;
Xia, XJ
;
Welch, KO
;
Blanton, SH
, et al.
소스
GENETICS IN MEDICINE
; JUL-AUG 2003, 5 4, p295-p303, 9p.
Full Text (ScienceDirect)
Full Text (ScienceDirect O/A)
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17 . Academic Journal
Chudley-McCullough syndrome: Expanded phenotype and review of the literature
저자
by
Welch, KO
;
Tekin, M
;
Nance, WE
;
Blanton, SH
;
Arnos, KS
, et al.
소스
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
; MAY 15 2003, 119A 1, p71-p76, 6p.
Scopus
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17 . Academic Journal
A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qter
저자
by
Blanton, SH
;
Liang, CY
;
Cai, MW
;
Pandya, A
;
Du, LL
, et al.
소스
JOURNAL OF MEDICAL GENETICS
; AUG 2002, 39 8, p567-p570, 4p.
Full Text (BMJ Journals)
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17 . Academic Journal
Testing for genetic associations with the PAX gene family in a spina bifida population
저자
by
Volcik, KA
;
Blanton, SH
;
Kruzel, MC
;
Townsend, IT
;
Tyerman, GH
, et al.
소스
AMERICAN JOURNAL OF MEDICAL GENETICS
; JUL 1 2002, 110 3, p195-p202, 8p.
Scopus
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17 . Academic Journal
Testing for genetic associations in a spina bifida population: Analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defects
저자
by
Volcik, KA
;
Blanton, SH
;
Kruzel, MC
;
Townsend, IT
;
Tyerman, GH
, et al.
소스
AMERICAN JOURNAL OF MEDICAL GENETICS
; JUL 1 2002, 110 3, p203-p207, 5p.
Scopus
Web of Science
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17 . Academic Journal
Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa
저자
by
Bowne, SJ
;
Sullivan, LS
;
Blanton, SH
;
Cepko, CL
;
Blackshaw, S
, et al.
소스
HUMAN MOLECULAR GENETICS
; MAR 1 2002, 11 5, p559-p568, 10p.
Full Text (OUP)
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