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Human Mutation
|
January 1, 1997
Novel mutations of the P gene in type II oculocutaneous albinism (OCA2)
R A Spritz, S T Lee, K Fukai, et al.
Journal of Medical Genetics
|
October 12, 2001
Potential mapping of corneal dermoids to Xq24-qter
P Dar, A A Javed, M Ben-Yishay, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
October 29, 2010
Congenital megalourethra: prenatal diagnosis and postnatal/autopsy findings in 10 cases
H Amsalem, B Fitzgerald, S Keating, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine
|
October 12, 2000
Fetal cardiac dextroposition in the absence of an intrathoracic mass: sign of significant right lung hypoplasia
M M Abdullah, R V Lacro, J Smallhorn, et al.
AJNR. American Journal of Neuroradiology
|
April 7, 2018
Characteristic MR Imaging Findings of the Neonatal Brain in RASopathies
M N Cizmeci, M Lequin, K D Lichtenbelt, et al.
Nature Genetics
|
October 31, 2001
A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome
L R Osborne, M Li, B Pober, et al.
Neurology
|
March 4, 1998
Pedigree analysis of French Canadian families with T14484C Leber's hereditary optic neuropathy
C Macmillan, T Kirkham, K Fu, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
March 21, 2020
Long-term postnatal outcome of fetuses with prenatally suspected septo-optic dysplasia
S Shinar, S Blaser, D Chitayat, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
April 8, 2015
Diagnostic utility of microarray testing in pregnancy loss
J A Rosenfeld, M E Tucker, L F Escobar, et al.
Neuroradiology
|
August 13, 2016
Validation of the finding of hypertrophy of the clava in infantile neuroaxonal dystrophy/PLA2G6 by biometric analysis
A Al-Maawali, G Yoon, A S Feigenbaum, et al.
Page
of 22
Search research articles
Search
Showing results (171-180 of 211) with videos related to
Sort By:
Page
of 22
Human Mutation
|
January 1, 1997
Novel mutations of the P gene in type II oculocutaneous albinism (OCA2)
R A Spritz, S T Lee, K Fukai, et al.
Journal of Medical Genetics
|
October 12, 2001
Potential mapping of corneal dermoids to Xq24-qter
P Dar, A A Javed, M Ben-Yishay, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
October 29, 2010
Congenital megalourethra: prenatal diagnosis and postnatal/autopsy findings in 10 cases
H Amsalem, B Fitzgerald, S Keating, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine
|
October 12, 2000
Fetal cardiac dextroposition in the absence of an intrathoracic mass: sign of significant right lung hypoplasia
M M Abdullah, R V Lacro, J Smallhorn, et al.
AJNR. American Journal of Neuroradiology
|
April 7, 2018
Characteristic MR Imaging Findings of the Neonatal Brain in RASopathies
M N Cizmeci, M Lequin, K D Lichtenbelt, et al.
Nature Genetics
|
October 31, 2001
A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome
L R Osborne, M Li, B Pober, et al.
Neurology
|
March 4, 1998
Pedigree analysis of French Canadian families with T14484C Leber's hereditary optic neuropathy
C Macmillan, T Kirkham, K Fu, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
March 21, 2020
Long-term postnatal outcome of fetuses with prenatally suspected septo-optic dysplasia
S Shinar, S Blaser, D Chitayat, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
April 8, 2015
Diagnostic utility of microarray testing in pregnancy loss
J A Rosenfeld, M E Tucker, L F Escobar, et al.
Neuroradiology
|
August 13, 2016
Validation of the finding of hypertrophy of the clava in infantile neuroaxonal dystrophy/PLA2G6 by biometric analysis
A Al-Maawali, G Yoon, A S Feigenbaum, et al.
Page
of 22