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Familial isolated clubfoot is associated with recurrent chromosome 17q23.1q23.2 microduplications containing TBX4. [electronic resource] by
- Alvarado, David M
- Aferol, Hyuliya
- McCall, Kevin
- Huang, Jason B
- Techy, Matthew
- Buchan, Jillian
- Cady, Janet
- Gonzales, Patrick R
- Dobbs, Matthew B
- Gurnett, Christina A
Producer: 20100728
In:
American journal of human genetics vol. 87
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126.
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127.
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What Factors Influence Union and Refracture of Congenital Pseudarthrosis of the Tibia? A Multicenter Long-term Study. [electronic resource] by
- Shah, Hitesh
- Joseph, Benjamin
- Nair, Binu V S
- Kotian, Devaki B
- Choi, In Ho
- Richards, Benjamin Stephens
- Johnston, Charles
- Madhuri, Vrisha
- Dobbs, Matthew B
- Dahl, Mark
Producer: 20181022
In:
Journal of pediatric orthopedics vol. 38
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128.
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Obex position is associated with syringomyelia and use of posterior fossa decompression among patients with Chiari I malformation. [electronic resource] by
- Haller, Gabe
- Sadler, Brooke
- Kuensting, Timothy
- Lakshman, Nivan
- Greenberg, Jacob K
- Strahle, Jennifer M
- Park, Tae Sung
- Dobbs, Matthew B
- Gurnett, Christina A
- Limbrick, David D
Publication details: Journal of neurosurgery. Pediatrics 07 2020
In:
Journal of neurosurgery. Pediatrics vol. 26
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129.
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Pitx1 haploinsufficiency causes clubfoot in humans and a clubfoot-like phenotype in mice. [electronic resource] by
- Alvarado, David M
- McCall, Kevin
- Aferol, Hyuliya
- Silva, Matthew J
- Garbow, Joel R
- Spees, William M
- Patel, Tarpit
- Siegel, Marilyn
- Dobbs, Matthew B
- Gurnett, Christina A
Producer: 20120123
In:
Human molecular genetics vol. 20
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130.
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131.
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HOXD10 M319K mutation in a family with isolated congenital vertical talus. [electronic resource] by
- Dobbs, Matthew B
- Gurnett, Christina A
- Pierce, Brandon
- Exner, G Ulrich
- Robarge, Jason
- Morcuende, Jose A
- Cole, William G
- Templeton, Peter A
- Foster, Bruce
- Bowcock, Anne M
Producer: 20060413
In:
Journal of orthopaedic research : official publication of the Orthopaedic Research Society vol. 24
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132.
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Genetic Risk for Aortic Aneurysm in Adolescent Idiopathic Scoliosis. [electronic resource] by
- Haller, Gabe
- Alvarado, David M
- Willing, Marcia C
- Braverman, Alan C
- Bridwell, Keith H
- Kelly, Michael
- Lenke, Lawrence G
- Luhmann, Scott J
- Gurnett, Christina A
- Dobbs, Matthew B
Producer: 20151123
In:
The Journal of bone and joint surgery. American volume vol. 97
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133.
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Genome-wide association study identifies new disease loci for isolated clubfoot. [electronic resource] by
- Zhang, Tian-Xiao
- Haller, Gabe
- Lin, Peng
- Alvarado, David M
- Hecht, Jacqueline T
- Blanton, Susan H
- Stephens Richards, B
- Rice, John P
- Dobbs, Matthew B
- Gurnett, Christina A
Producer: 20150512
In:
Journal of medical genetics vol. 51
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134.
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Editorial: The Complexity of Reporting Race and Ethnicity in Orthopaedic Research. [electronic resource] by
- Leopold, Seth S
- Beadling, Lee
- Calabro, Anthony M
- Dobbs, Matthew B
- Gebhardt, Mark C
- Gioe, Terence J
- Manner, Paul A
- Porcher, Raphaël
- Rimnac, Clare M
- Wongworawat, Montri D
Producer: 20190530
In:
Clinical orthopaedics and related research vol. 476
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135.
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Variants in genes that encode muscle contractile proteins influence risk for isolated clubfoot. [electronic resource] by
- Weymouth, Katelyn S
- Blanton, Susan H
- Bamshad, Michael J
- Beck, Anita E
- Alvarez, Christine
- Richards, Steve
- Gurnett, Christina A
- Dobbs, Matthew B
- Barnes, Douglas
- Mitchell, Laura E
- Hecht, Jacqueline T
Producer: 20120209
In:
American journal of medical genetics. Part A vol. 155A
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136.
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CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis. [electronic resource] by
- Gao, Xiaochong
- Gordon, Derek
- Zhang, Dongping
- Browne, Richard
- Helms, Cynthia
- Gillum, Joseph
- Weber, Samuel
- Devroy, Shonn
- Swaney, Saralove
- Dobbs, Matthew
- Morcuende, Jose
- Sheffield, Val
- Lovett, Michael
- Bowcock, Anne
- Herring, John
- Wise, Carol
Producer: 20070611
In:
American journal of human genetics vol. 80
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137.
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A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosis. [electronic resource] by
- Haller, Gabe
- Alvarado, David
- Mccall, Kevin
- Yang, Ping
- Cruchaga, Carlos
- Harms, Matthew
- Goate, Alison
- Willing, Marcia
- Morcuende, Jose A
- Baschal, Erin
- Miller, Nancy H
- Wise, Carol
- Dobbs, Matthew B
- Gurnett, Christina A
Producer: 20160923
In:
Human molecular genetics vol. 25
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138.
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Adolescent idiopathic scoliosis. [electronic resource] by
- Cheng, Jack C
- Castelein, René M
- Chu, Winnie C
- Danielsson, Aina J
- Dobbs, Matthew B
- Grivas, Theodoros B
- Gurnett, Christina A
- Luk, Keith D
- Moreau, Alain
- Newton, Peter O
- Stokes, Ian A
- Weinstein, Stuart L
- Burwell, R Geoffrey
Producer: 20180119
In:
Nature reviews. Disease primers vol. 1
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139.
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Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis. [electronic resource] by
- Baschal, Erin E
- Wethey, Cambria I
- Swindle, Kandice
- Baschal, Robin M
- Gowan, Katherine
- Tang, Nelson L S
- Alvarado, David M
- Haller, Gabe E
- Dobbs, Matthew B
- Taylor, Matthew R G
- Gurnett, Christina A
- Jones, Kenneth L
- Miller, Nancy H
Producer: 20151117
In:
G3 (Bethesda, Md.) vol. 5
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140.
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Bracing in Adolescent Idiopathic Scoliosis Trial (BrAIST): Development and Validation of a Prognostic Model in Untreated Adolescent Idiopathic Scoliosis Using the Simplified Skeletal Maturity System. [electronic resource] by
- Dolan, Lori A
- Weinstein, Stuart L
- Abel, Mark F
- Bosch, Patrick P
- Dobbs, Matthew B
- Farber, Tyler O
- Halsey, Matthew F
- Hresko, M Timothy
- Krengel, Walter F
- Mehlman, Charles T
- Sanders, James O
- Schwend, Richard M
- Shah, Suken A
- Verma, Kushagra
Producer: 20200506
In:
Spine deformity vol. 7
Availability: No items available.
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