A Spectrum of FOXC1 Mutations Suggests Gene Dosage as a Mechanism for Developmental Defects of the Anterior Chamber of the Eye
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 (01.02.2001)
Published in American journal of human genetics (01.02.2001)
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The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
Sheffield, Val C, Nishimura, Darryl Y, Swiderski, Ruth E, Alward, Wallace L. M, Searby, Charles C, Patil, Shivanand R, Bennet, Steven R, Kanis, Adam B, Gastier, Julie M, Stone, Edwin M
Published in Nature genetics (01.06.1998)
Published in Nature genetics (01.06.1998)
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Homozygosity Mapping of Achromatopsia to Chromosome 2 Using DNA Pooling
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 (01.05.1997)
Published in Human molecular genetics (01.05.1997)
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Antenatal sonographic diagnosis of club foot with particular attention to the implications and outcomes of isolated club foot
Rijhsinghani, A., Yankowitz, J., Kanis, A. B., Mueller, G. M., Yankowitz, D. K., Williamson, R. A.
Published in Ultrasound in obstetrics & gynecology (01.08.1998)
Published in Ultrasound in obstetrics & gynecology (01.08.1998)
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Genomic organization, 5'-flanking region, and chromosomal localization of the human RGS3 gene
CHATTERJEE, T. K, EAPEN, A, KANIS, A. B, FISHER, R. A
Published in Genomics (San Diego, Calif.) (15.10.1997)
Published in Genomics (San Diego, Calif.) (15.10.1997)
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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
Schmidt, Nicole, Van Dyke, Don C, Keppler-Noreuil, Kim, Muilenburg, Ann, Patil, Shivanand, Kanis, Adam B
Published in Developmental medicine and child neurology (01.02.2001)
Published in Developmental medicine and child neurology (01.02.2001)
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PRENATAL ULTRASOUND FINDINGS IN HYDROLETHALUS: CONTINUING DIFFICULTIES IN DIAGNOSIS
NORGARD, MICHAEL, YANKOWITZ, JEROME, RHEAD, WILLIAM, KANIS, ADAM B., HALL, BRYAN D.
Published in Prenatal diagnosis (01.02.1996)
Published in Prenatal diagnosis (01.02.1996)
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Nonsyndromic congenital retinal nonattachment gene maps to human chromosome band 10q21
Ghiasvand, N M, Kanis, A B, Helms, C, Sheffield, V C, Stone, E M, Donis-Keller, H
Published in American journal of medical genetics (17.01.2000)
Published in American journal of medical genetics (17.01.2000)
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Short tandem repeat polymorphic markers for the rat genome from marker-selected libraries
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 (01.12.1998)
Published in Mammalian genome (01.12.1998)
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Exclusion of AR-CHED from the chromosome 20 region containing the PPMD and AD-CHED loci
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 (1999)
Published in Ophthalmic genetics (1999)
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