Search research articles
Contact Us
Filters
Showing results (11-20 of 56) with videos related to
Page
of 6
Sort By:
American Journal of Medical Genetics. Part A
|
February 27, 2010
c. 595-596 insC of FOXC2 underlies lymphedema, distichiasis, ptosis, ankyloglossia, and Robin sequence in a Thai patient
Pranoot Tanpaiboon, Piranit Kantaputra, Karn Wejathikul, et al.
American Journal of Medical Genetics. Part A
|
September 17, 2004
Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies: confirmation of a new syndrome
Piranit N Kantaputra, Pranoot Tanpaiboon, Kevalee Unachak, et al.
European Journal of Dermatology : EJD
|
June 25, 2008
Two novel EBP mutations in Conradi-Hünermann-Happle syndrome
Surasawadee Ausavarat, Pranoot Tanpaiboon, Siraprapa Tongkobpetch, et al.
European Journal of Medical Genetics
|
August 12, 2020
A patient with atypical presentation of chronic hepatosteatosis harboring a novel variant in the CPT1A gene
Ponghatai Boonsimma, Kathleen Crosby, Parvathi Mohan, et al.
Antiviral Therapy
|
May 29, 2009
Plasma efavirenz concentrations and the association with CYP2B6-516G >T polymorphism in HIV-infected Thai children
Thanyawee Puthanakit, Pranoot Tanpaiboon, Linda Aurpibul, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
November 19, 2015
Isolated methylmalonic acidemia with unusual presentation mimicking diabetic ketoacidosis
Prapai Dejkhamron, Karn Wejapikul, Kevalee Unachak, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 26, 2017
Do the data really support ordering fragile X testing as a first-tier test without clinical features?
Veronique Weinstein, Pranoot Tanpaiboon, Kimberly A Chapman, et al.
American Journal of Medical Genetics. Part A
|
July 17, 2009
Expanding the phenotypic spectrum of acro-cardio-facial syndrome (ACFS): Exclusion of P63 mutation
Pranoot Tanpaiboon, Rekwan Sittiwangkul, Prapai Dejkhamron, et al.
Molecular Genetics and Metabolism Reports
|
January 15, 2024
Plasma arginine levels in arginase deficiency in the "real world"
Pranoot Tanpaiboon, Yue Huang, Judy Z Louie, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet
|
April 5, 2008
Thyroid functions in children with Down's syndrome
Kevalee Unachak, Pranoot Tanpaiboon, Yupada Pongprot, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 56) with videos related to
Sort By:
Page
of 6
American Journal of Medical Genetics. Part A
|
February 27, 2010
c. 595-596 insC of FOXC2 underlies lymphedema, distichiasis, ptosis, ankyloglossia, and Robin sequence in a Thai patient
Pranoot Tanpaiboon, Piranit Kantaputra, Karn Wejathikul, et al.
American Journal of Medical Genetics. Part A
|
September 17, 2004
Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies: confirmation of a new syndrome
Piranit N Kantaputra, Pranoot Tanpaiboon, Kevalee Unachak, et al.
European Journal of Dermatology : EJD
|
June 25, 2008
Two novel EBP mutations in Conradi-Hünermann-Happle syndrome
Surasawadee Ausavarat, Pranoot Tanpaiboon, Siraprapa Tongkobpetch, et al.
European Journal of Medical Genetics
|
August 12, 2020
A patient with atypical presentation of chronic hepatosteatosis harboring a novel variant in the CPT1A gene
Ponghatai Boonsimma, Kathleen Crosby, Parvathi Mohan, et al.
Antiviral Therapy
|
May 29, 2009
Plasma efavirenz concentrations and the association with CYP2B6-516G >T polymorphism in HIV-infected Thai children
Thanyawee Puthanakit, Pranoot Tanpaiboon, Linda Aurpibul, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
November 19, 2015
Isolated methylmalonic acidemia with unusual presentation mimicking diabetic ketoacidosis
Prapai Dejkhamron, Karn Wejapikul, Kevalee Unachak, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 26, 2017
Do the data really support ordering fragile X testing as a first-tier test without clinical features?
Veronique Weinstein, Pranoot Tanpaiboon, Kimberly A Chapman, et al.
American Journal of Medical Genetics. Part A
|
July 17, 2009
Expanding the phenotypic spectrum of acro-cardio-facial syndrome (ACFS): Exclusion of P63 mutation
Pranoot Tanpaiboon, Rekwan Sittiwangkul, Prapai Dejkhamron, et al.
Molecular Genetics and Metabolism Reports
|
January 15, 2024
Plasma arginine levels in arginase deficiency in the "real world"
Pranoot Tanpaiboon, Yue Huang, Judy Z Louie, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet
|
April 5, 2008
Thyroid functions in children with Down's syndrome
Kevalee Unachak, Pranoot Tanpaiboon, Yupada Pongprot, et al.
Page
of 6