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Hazel Perry

Showing results (1-10 of 12) with videos related to

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American Journal of Medical Genetics. Part A|August 25, 2010
A novel EFNB1 mutation (c.712delG) in a family with craniofrontonasal syndrome and diaphragmatic herniaJacob Hogue, Suma Shankar, Hazel Perry, et al.
The Journal of Craniofacial Surgery|September 22, 2010
Clefting in trisomy 9p patients: genotype-phenotype correlation using microarray comparative genomic hybridizationAngie Jelin, Hazel Perry, Jacob Hogue, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
Novel FGFR2 deletion in a patient with Beare-Stevenson-like syndromeAnne Slavotinek, Howard Crawford, Mahin Golabi, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|June 29, 2019
Case Report of Floating-Harbor Syndrome With Bilateral Cleft LipJaemin Ko, Jason H Pomerantz, Hazel Perry, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP|May 11, 2006
Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutationFaraz Farzin, Hazel Perry, David Hessl, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|August 19, 2024
Genetic Testing in Craniofacial Care: Development of Algorithms for Testing Patients with Orofacial Clefting, Branchial Arch Anomalies, and CraniosynostosisEmily R Gallagher, Penny Chow, Maria R Mills, et al.
Human Molecular Genetics|May 9, 2015
DLX4 is associated with orofacial clefting and abnormal jaw developmentDi Wu, Shyamali Mandal, Alex Choi, et al.
American Journal of Medical Genetics. Part A|April 18, 2015
Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencingYuri A Zarate, Hazel Perry, Tawfeg Ben-Omran, et al.
NPJ Genomic Medicine|October 13, 2021
Publisher Correction: Application of full-genome analysis to diagnose rare monogenic disordersJoseph T Shieh, Monica Penon-Portmann, Karen H Y Wong, et al.
NPJ Genomic Medicine|September 24, 2021
Application of full-genome analysis to diagnose rare monogenic disordersJoseph T Shieh, Monica Penon-Portmann, Karen H Y Wong, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics. Part A|August 25, 2010
A novel EFNB1 mutation (c.712delG) in a family with craniofrontonasal syndrome and diaphragmatic herniaJacob Hogue, Suma Shankar, Hazel Perry, et al.
The Journal of Craniofacial Surgery|September 22, 2010
Clefting in trisomy 9p patients: genotype-phenotype correlation using microarray comparative genomic hybridizationAngie Jelin, Hazel Perry, Jacob Hogue, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
Novel FGFR2 deletion in a patient with Beare-Stevenson-like syndromeAnne Slavotinek, Howard Crawford, Mahin Golabi, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|June 29, 2019
Case Report of Floating-Harbor Syndrome With Bilateral Cleft LipJaemin Ko, Jason H Pomerantz, Hazel Perry, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP|May 11, 2006
Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutationFaraz Farzin, Hazel Perry, David Hessl, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|August 19, 2024
Genetic Testing in Craniofacial Care: Development of Algorithms for Testing Patients with Orofacial Clefting, Branchial Arch Anomalies, and CraniosynostosisEmily R Gallagher, Penny Chow, Maria R Mills, et al.
Human Molecular Genetics|May 9, 2015
DLX4 is associated with orofacial clefting and abnormal jaw developmentDi Wu, Shyamali Mandal, Alex Choi, et al.
American Journal of Medical Genetics. Part A|April 18, 2015
Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencingYuri A Zarate, Hazel Perry, Tawfeg Ben-Omran, et al.
NPJ Genomic Medicine|October 13, 2021
Publisher Correction: Application of full-genome analysis to diagnose rare monogenic disordersJoseph T Shieh, Monica Penon-Portmann, Karen H Y Wong, et al.
NPJ Genomic Medicine|September 24, 2021
Application of full-genome analysis to diagnose rare monogenic disordersJoseph T Shieh, Monica Penon-Portmann, Karen H Y Wong, et al.
Pageof 2