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American Journal of Medical Genetics
|
December 11, 1996
Autosomal dominant inheritance of hypothalamic hamartoma associated with polysyndactyly: heterogeneity or variable expressivity?
T A Grebe, C Clericuzio
American Journal of Medical Genetics
|
November 15, 2000
Neurologic and gastrointestinal dysfunction in cardio-facio-cutaneous syndrome: identification of a severe phenotype
T A Grebe, C Clericuzio
Ultrasonics
|
March 29, 2001
Application of time delay spectrometry for rough surface characterization
P C Pedersen, A Grebe
American Journal of Medical Genetics. Part A
|
July 12, 2023
15q26.3 deletions distal to IGF1R cause growth retardation, congenital heart defect and skeletal anomalies: Case report and review of literature
Theru A Sivakumaran, Theresa A Grebe
The Journal of Pediatrics
|
June 1, 1993
Toxic reaction to salicylate in a newborn infant: similarities to neonatal sepsis
M L Buck, T A Grebe, G R Bond
American Journal of Medical Genetics. Part A
|
August 23, 2015
Chronic pain in Noonan Syndrome: A previously unreported but common symptom
Sravanthi Vegunta, Richard Cotugno, Amber Williamson, et al.
American Journal of Medical Genetics. Part A
|
March 3, 2025
First Report of Phosphoglycerate Kinase Deficiency in a Dinè Child With Review of Current Literature
Ariel Hierholzer, Jillian Mador, Rachna Guntu, et al.
Journal of Child Neurology
|
June 11, 2015
Progressive Movement Disorder in Brothers Carrying a GNAO1 Mutation Responsive to Deep Brain Stimulation
Neil Kulkarni, Sha Tang, Ratan Bhardwaj, et al.
Molecular Genetics and Metabolism Reports
|
January 11, 2017
An atypical presentation of ACAD9 deficiency: Diagnosis by whole exome sequencing broadens the phenotypic spectrum and alters treatment approach
H K Aintablian, V Narayanan, N Belnap, et al.
American Journal of Medical Genetics
|
September 1, 1992
7p deletion syndrome: an adult with mild manifestations
T A Grebe, M A Stevens, K Byrne-Essif, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 44) with videos related to
Sort By:
Page
of 5
American Journal of Medical Genetics
|
December 11, 1996
Autosomal dominant inheritance of hypothalamic hamartoma associated with polysyndactyly: heterogeneity or variable expressivity?
T A Grebe, C Clericuzio
American Journal of Medical Genetics
|
November 15, 2000
Neurologic and gastrointestinal dysfunction in cardio-facio-cutaneous syndrome: identification of a severe phenotype
T A Grebe, C Clericuzio
Ultrasonics
|
March 29, 2001
Application of time delay spectrometry for rough surface characterization
P C Pedersen, A Grebe
American Journal of Medical Genetics. Part A
|
July 12, 2023
15q26.3 deletions distal to IGF1R cause growth retardation, congenital heart defect and skeletal anomalies: Case report and review of literature
Theru A Sivakumaran, Theresa A Grebe
The Journal of Pediatrics
|
June 1, 1993
Toxic reaction to salicylate in a newborn infant: similarities to neonatal sepsis
M L Buck, T A Grebe, G R Bond
American Journal of Medical Genetics. Part A
|
August 23, 2015
Chronic pain in Noonan Syndrome: A previously unreported but common symptom
Sravanthi Vegunta, Richard Cotugno, Amber Williamson, et al.
American Journal of Medical Genetics. Part A
|
March 3, 2025
First Report of Phosphoglycerate Kinase Deficiency in a Dinè Child With Review of Current Literature
Ariel Hierholzer, Jillian Mador, Rachna Guntu, et al.
Journal of Child Neurology
|
June 11, 2015
Progressive Movement Disorder in Brothers Carrying a GNAO1 Mutation Responsive to Deep Brain Stimulation
Neil Kulkarni, Sha Tang, Ratan Bhardwaj, et al.
Molecular Genetics and Metabolism Reports
|
January 11, 2017
An atypical presentation of ACAD9 deficiency: Diagnosis by whole exome sequencing broadens the phenotypic spectrum and alters treatment approach
H K Aintablian, V Narayanan, N Belnap, et al.
American Journal of Medical Genetics
|
September 1, 1992
7p deletion syndrome: an adult with mild manifestations
T A Grebe, M A Stevens, K Byrne-Essif, et al.
Page
of 5