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/vufind/Search/Results?lookfor=%22Li%2C+Madeline%22&type=Person&page=14
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PubPharm (136)
131
Imprinting Status of 11p15 Genes in Beckwith-Wiedemann Syndrome Patients with CDKN1C Mutations
enthalten in:
Genomics
| 2001
von
Li, M.
|
Squire, J.
|
Shuman, C.
| +5
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132
GPC3 Mutation Analysis in a Spectrum of Patients With Overgrowth Expands the Phenotype of Simpson-Golabi-Behmel Syndrome Published online 2 July 2001
enthalten in:
American journal of medical genetics
| 2001
von
Li, M.
|
Shuman, C.
|
Fei, Y.
| +9
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133
Alterations of H19 Imprinting and IGF2 Replication Timing Are Infrequent in Beckwith-Wiedemann Syndrome
enthalten in:
Genomics
| 2000
von
Squire, J.
|
Li, M.
|
Perlikowski, S.
| +4
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134
Molecular Genetics Of Wiedemann-Beckwith Syndrome
enthalten in:
American journal of medical genetics
| 1998
von
Li, M.
|
Squire, J.
|
Weksberg, R.
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135
Expression of OCI-5-Glypican 3 during Intestinal Morphogenesis: Regulation by Cell Shape in Intestinal Epithelial Cells
enthalten in:
Experimental cell research
| 1997
von
Li, M.
|
Choo, B.
|
Wong, Z.
| +2
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136
Genetics - Molecular genetics of Beckwith-Weidman syndrome
enthalten in:
Current opinion in pediatrics
| 1997
von
Li, M.
|
Squire, J.
|
Weksberg, R.
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