Search research articles
Contact Us
Filters
Showing results (1-10 of 68) with videos related to
Page
of 7
Sort By:
Psychoneuroendocrinology
|
January 29, 2017
Maternal salivary cortisone to cortisol ratio in late pregnancy: An improved method for predicting offspring birth weight
Meredith Wilson, Zaneta Thayer
Annals of Human Biology
|
September 12, 2018
Impact of acculturation on depression, perceived stress and self-esteem in young Middle Eastern American adults
Meredith Wilson, Zaneta Thayer
American Journal of Medical Genetics. Part A
|
December 22, 2015
Sleep disturbance in Mowat-Wilson syndrome
Elizabeth Evans, David Mowat, Meredith Wilson, et al.
British Journal of Haematology
|
June 3, 2006
The identification of a recurrent phosphoglycerate kinase mutation associated with chronic haemolytic anaemia and neurological dysfunction in a family from USA
Jonathan M Flanagan, Melissa Rhodes, Meredith Wilson, et al.
Journal of Paediatrics and Child Health
|
July 15, 2005
Neonatal nasal obstruction and a single maxillary central incisor
John Levison, Katherine Neas, Meredith Wilson, et al.
American Journal of Medical Genetics. Part A
|
June 29, 2016
Recurrence of split hand/foot malformation, cleft lip/palate, and severe urogenital abnormalities due to germline mosaicism for TP63 mutation
Annabelle Enriquez, Michael Krivanek, Ricarda Flöttmann, et al.
Blood Cells, Molecules & Diseases
|
August 6, 2010
Enzyme replacement therapy "drug holiday": results from an unexpected shortage of an orphan drug supply in Australia
Jack Goldblatt, Janice M Fletcher, Jim McGill, et al.
American Journal of Medical Genetics. Part A
|
January 17, 2012
The behavioral phenotype of Mowat-Wilson syndrome
Elizabeth Evans, Stewart Einfeld, David Mowat, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
September 24, 2015
A negative waveform in the scotopic response in a patient with phosphoglycerate kinase deficiency: a visual electrophysiology report
Safinaz Mohd Khialdin, John Grigg, Neil Rowe, et al.
American Journal of Medical Genetics. Part A
|
February 4, 2005
Diagnostic FISH probes for del(17)(p11.2p11.2) associated with Smith-Magenis syndrome should contain the RAI1 gene
Christopher N Vlangos, Meredith Wilson, Jan Blancato, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 68) with videos related to
Sort By:
Page
of 7
Psychoneuroendocrinology
|
January 29, 2017
Maternal salivary cortisone to cortisol ratio in late pregnancy: An improved method for predicting offspring birth weight
Meredith Wilson, Zaneta Thayer
Annals of Human Biology
|
September 12, 2018
Impact of acculturation on depression, perceived stress and self-esteem in young Middle Eastern American adults
Meredith Wilson, Zaneta Thayer
American Journal of Medical Genetics. Part A
|
December 22, 2015
Sleep disturbance in Mowat-Wilson syndrome
Elizabeth Evans, David Mowat, Meredith Wilson, et al.
British Journal of Haematology
|
June 3, 2006
The identification of a recurrent phosphoglycerate kinase mutation associated with chronic haemolytic anaemia and neurological dysfunction in a family from USA
Jonathan M Flanagan, Melissa Rhodes, Meredith Wilson, et al.
Journal of Paediatrics and Child Health
|
July 15, 2005
Neonatal nasal obstruction and a single maxillary central incisor
John Levison, Katherine Neas, Meredith Wilson, et al.
American Journal of Medical Genetics. Part A
|
June 29, 2016
Recurrence of split hand/foot malformation, cleft lip/palate, and severe urogenital abnormalities due to germline mosaicism for TP63 mutation
Annabelle Enriquez, Michael Krivanek, Ricarda Flöttmann, et al.
Blood Cells, Molecules & Diseases
|
August 6, 2010
Enzyme replacement therapy "drug holiday": results from an unexpected shortage of an orphan drug supply in Australia
Jack Goldblatt, Janice M Fletcher, Jim McGill, et al.
American Journal of Medical Genetics. Part A
|
January 17, 2012
The behavioral phenotype of Mowat-Wilson syndrome
Elizabeth Evans, Stewart Einfeld, David Mowat, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
September 24, 2015
A negative waveform in the scotopic response in a patient with phosphoglycerate kinase deficiency: a visual electrophysiology report
Safinaz Mohd Khialdin, John Grigg, Neil Rowe, et al.
American Journal of Medical Genetics. Part A
|
February 4, 2005
Diagnostic FISH probes for del(17)(p11.2p11.2) associated with Smith-Magenis syndrome should contain the RAI1 gene
Christopher N Vlangos, Meredith Wilson, Jan Blancato, et al.
Page
of 7