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Keyword [Opitz syndrome]
Result: 1 - 7 | Page: 1 of 1
1.
Genetic Disorders Of Cholesterol Biosynthesis-Pathophysiological Studies Of Smith-Lemli-Opitz Syndrome
2.
The Cellular Function Of MID2 And Its Potential Role In The Pathogenesis Of Opitz Syndrome
3.
Expression Pattern Of Mid1/mid2 During Mouse Early Development
4.
Chemical, biochemical, and bioanalytical studies of sterols and isoprenoids: Smith-Lemli-Opitz syndrome, Langer-Giedion syndrome, activation of meiosis, nuclear orphan receptor LXRalpha and cytochrome P450s
5.
X-linked Opitz Syndrome protein, MID1, and its effects on cell adhesion force and protein interactions
6.
Assessment of the Whole Body Cholesterol Pool Size in Smith-Lemli-Opitz Syndrome Patients Receiving Cholesterol Supplementation Alone or Combined with Simvastatin
7.
The Effect Of Opitz Syndrome Gene MID1 On Early Craniofacial Development And Its Molecular Function
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