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Search Results - Kanis, Adam B
Search Results - Kanis, Adam B
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A Spectrum of FOXC1 Mutations Suggests Gene Dosage as a Mechanism for Developmental Defects of the Anterior Chamber of the Eye
by
Nishimura, Darryl Y.
,
Searby, Charles C.
,
Alward, Wallace L.
,
Walton, David
,
Craig, Jamie E.
,
Mackey, David A.
,
Kawase, Kazuhide
,
Kanis, Adam B.
,
Patil, Shivanand R.
,
Stone, Edwin M.
,
Sheffield, Val C.
Published in
American journal of human genetics
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Cochlear implantation in deafness-dystonia-optic neuronopathy (DDON) syndrome
by
Brookes, James T
,
Kanis, Adam B
,
Tan, Lih Yeen
,
Tranebjærg, Lisbeth
,
Vore, Abram
,
Smith, Richard J.H
Published in
International journal of pediatric otorhinolaryngology
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Short tandem repeat polymorphic markers for the rat genome from marker-selected libraries
by
Walder, R Y
,
Garrett, M R
,
McClain, A M
,
Beck, G E
,
Brennan, T M
,
Kramer, N A
,
Kanis, A B
,
Mark, A L
,
Rapp, J P
,
Sheffield, V C
Published in
Mammalian genome
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Developmental delay and multiple congenital anomalies in a child with a unique combination of partial monosomy 18 and partial trisomy 16
by
Schmidt, Nicole
,
Van Dyke, Don C
,
Keppler-Noreuil, Kim
,
Muilenburg, Ann
,
Patil, Shivanand
,
Kanis, Adam B
Published in
Developmental medicine and child neurology
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Homozygosity Mapping of Achromatopsia to Chromosome 2 Using DNA Pooling
by
Arbour, Nancy C.
,
Zlotogora, Joel
,
Knowlton, Robert G.
,
Merin, Saul
,
Rosenmann, Ada
,
Kanis, Adam B.
,
Rokhlina, Tatiana
,
Stone, Edwin M.
,
Sheffield, Val C.
Published in
Human molecular genetics
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Developmental delay and multiple congenital anomalies in a child with a unique combination of partial monosomy 18 and partial trisomy 16
by
Schmidt, Nicole
,
Dyke, Don C Van
,
Keppler‐Noreuil, Kim
,
Muilenburg, Ann
,
Patil, Shivanand
,
Kanis, Adam B
Published in
Developmental medicine and child neurology
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Genomic organization, 5'-flanking region, and chromosomal localization of the human RGS3 gene
by
CHATTERJEE, T. K
,
EAPEN, A
,
KANIS, A. B
,
FISHER, R. A
Published in
Genomics (San Diego, Calif.)
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Genomic Organization, 5′-Flanking Region, and Chromosomal Localization of the HumanRGS3Gene
by
Chatterjee, Tapan K.
,
Eapen, Alex
,
Kanis, Adam B.
,
Fisher, Rory A.
Published in
Genomics (San Diego, Calif.)
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Exclusion of AR-CHED from the chromosome 20 region containing the PPMD and AD-CHED loci
by
Kanis, Adam B.
,
Al-Rajhi, Ali A.
,
Taylor, Christine M.
,
Mathers, William D.
,
Folberg, Robert
,
Nishimura, Darryl Y.
,
Sheffield, Val C.
,
Stone, Edwin M.
Published in
Ophthalmic genetics
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Interpretation and use of FRAX in clinical practice
by
Kanis, J. A.
,
Hans, D.
,
Cooper, C.
,
Baim, S.
,
Bilezikian, J. P.
,
Binkley, N.
,
Cauley, J. A.
,
Compston, J. E.
,
Dawson-Hughes, B.
,
El-Hajj Fuleihan, G.
,
Johansson, H.
,
Leslie, W. D.
,
Lewiecki, E. M.
,
Luckey, M.
,
Oden, A.
,
Papapoulos, S. E.
,
Poiana, C.
,
Rizzoli, R.
,
Wahl, D. A.
,
McCloskey, E. V.
Published in
Osteoporosis international
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