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John M Graham

Showing results (91-100 of 208) with videos related to

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American Journal of Medical Genetics. Part A|January 8, 2005
An epidemiological analysis of CHARGE syndrome: preliminary results from a Canadian studyKarina A Issekutz, John M Graham, Chitra Prasad, et al.
European Journal of Medical Genetics|December 29, 2019
De novo copy number variants and parental age: Is there an association?Isha Wadhawan, Yang Hai, Nastaran Foyouzi Yousefi, et al.
American Journal of Medical Genetics. Part A|April 23, 2003
Morphogenesis: Re: Clinical, natural history, and imaging information on patients included in reportsArt Aylsworth, John M Graham, Judith G Hall, et al.
European Journal of Medical Genetics|February 28, 2012
De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: a genomics approach to personalized medicineRyan E O'Leary, Jean C Shih, Keith Hyland, et al.
The Journal of Pediatrics|February 4, 2005
Management of deformational plagiocephaly: repositioning versus orthotic therapyJohn M Graham, Mayela Gomez, Andy Halberg, et al.
International Dental Journal|June 24, 2025
A Novel KDF1 Variant is Associated With Multiple Natal Teeth, Tooth Agenesis, and Root MaldevelopmentJohn M Graham, Pedro A Sanchez-Lara, Atsushi Ohazama, et al.
The Journal of Pediatrics|December 8, 2004
Clinical and behavioral features of patients with Borjeson-Forssman-Lehmann syndrome with mutations in PHF6Jeannie Visootsak, Beth Rosner, Elisabeth Dykens, et al.
European Journal of Medical Genetics|January 2, 2016
Early Infantile Epileptic Encephalopathy with a de novo variant in ZEB2 identified by exome sequencingNatalia Babkina, Joshua L Deignan, Hane Lee, et al.
Human Mutation|July 12, 2007
Multigene deletions on chromosome 20q13.13-q13.2 including SALL4 result in an expanded phenotype of Okihiro syndrome plus developmental delayWiktor Borozdin, John M Graham, Detlef Böhm, et al.
American Journal of Medical Genetics|November 29, 2002
Spectrum of dolichospondylic dysplasia: two new patients with distinctive findingsAlison M Elliott, John M Graham, Cynthia J R Curry, et al.
Pageof 21

Showing results (91-100 of 208) with videos related to

Sort By:
Pageof 21
American Journal of Medical Genetics. Part A|January 8, 2005
An epidemiological analysis of CHARGE syndrome: preliminary results from a Canadian studyKarina A Issekutz, John M Graham, Chitra Prasad, et al.
European Journal of Medical Genetics|December 29, 2019
De novo copy number variants and parental age: Is there an association?Isha Wadhawan, Yang Hai, Nastaran Foyouzi Yousefi, et al.
American Journal of Medical Genetics. Part A|April 23, 2003
Morphogenesis: Re: Clinical, natural history, and imaging information on patients included in reportsArt Aylsworth, John M Graham, Judith G Hall, et al.
European Journal of Medical Genetics|February 28, 2012
De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: a genomics approach to personalized medicineRyan E O'Leary, Jean C Shih, Keith Hyland, et al.
The Journal of Pediatrics|February 4, 2005
Management of deformational plagiocephaly: repositioning versus orthotic therapyJohn M Graham, Mayela Gomez, Andy Halberg, et al.
International Dental Journal|June 24, 2025
A Novel KDF1 Variant is Associated With Multiple Natal Teeth, Tooth Agenesis, and Root MaldevelopmentJohn M Graham, Pedro A Sanchez-Lara, Atsushi Ohazama, et al.
The Journal of Pediatrics|December 8, 2004
Clinical and behavioral features of patients with Borjeson-Forssman-Lehmann syndrome with mutations in PHF6Jeannie Visootsak, Beth Rosner, Elisabeth Dykens, et al.
European Journal of Medical Genetics|January 2, 2016
Early Infantile Epileptic Encephalopathy with a de novo variant in ZEB2 identified by exome sequencingNatalia Babkina, Joshua L Deignan, Hane Lee, et al.
Human Mutation|July 12, 2007
Multigene deletions on chromosome 20q13.13-q13.2 including SALL4 result in an expanded phenotype of Okihiro syndrome plus developmental delayWiktor Borozdin, John M Graham, Detlef Böhm, et al.
American Journal of Medical Genetics|November 29, 2002
Spectrum of dolichospondylic dysplasia: two new patients with distinctive findingsAlison M Elliott, John M Graham, Cynthia J R Curry, et al.
Pageof 21