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Article title matches
- Category:Lissencephaly (44 bytes)
1: List of pages with the keyword Lissencephaly
Page text matches
- 1uuj (6,370 bytes)
2: ==N-terminal domain of Lissencephaly-1 protein (Lis-1)==
24: ...ins the molecular basis of a low severity form of lissencephaly.
26: ...re of the N-terminal domain of the product of the lissencephaly gene Lis1 and its functional implications.,Kim MH... - 1mjd (6,000 bytes)
10: ... chromosomal aberration involving DCX is found in lissencephaly. Translocation t(X;2)(q22.3;p25.1).
25: ...Mutations in the gene encoding doublecortin cause lissencephaly in males and the 'double-cortex syndrome' in fema... - 1vyh (4,181 bytes)
23: ...rface of LIS1 contains sites of mutations causing lissencephaly and overlaps with a putative dynein binding surfa... - 2bqq (6,217 bytes)
10: ... chromosomal aberration involving DCX is found in lissencephaly. Translocation t(X;2)(q22.3;p25.1). - 8ru2 (3,078 bytes)
11: ...n malformation consisting of anterior-predominant lissencephaly. Other typical features include postnatal short s... - 2v66 (5,272 bytes)
24: ...ed lissencephaly sequence (ILS) and Miller-Dieker lissencephaly. The molecular basis of the interactions of Ndel1...
26: ...on with Lis1, the causal protein of Miller-Dieker lissencephaly.,Derewenda U, Tarricone C, Choi WC, Cooper DR, Lu... - 2v71 (3,992 bytes)
21: ...ed lissencephaly sequence (ILS) and Miller-Dieker lissencephaly. The molecular basis of the interactions of Ndel1...
23: ...on with Lis1, the causal protein of Miller-Dieker lissencephaly.,Derewenda U, Tarricone C, Choi WC, Cooper DR, Lu... - 3byh (3,441 bytes)
10: ...n malformation consisting of anterior-predominant lissencephaly. Other typical features include postnatal short s... - Category:Lissencephaly (44 bytes)
1: List of pages with the keyword Lissencephaly - 3lue (3,503 bytes)
10: ...n malformation consisting of anterior-predominant lissencephaly. Other typical features include postnatal short s... - 8rty (3,535 bytes)
11: ...n malformation consisting of anterior-predominant lissencephaly. Other typical features include postnatal short s... - 8fdt (4,183 bytes)
11: ...ller-Dieker syndrome;Subcortical band heterotopia;Lissencephaly due to LIS1 mutation;17p13.3 microduplication syn... - 8fdu (4,101 bytes)
11: ...ller-Dieker syndrome;Subcortical band heterotopia;Lissencephaly due to LIS1 mutation;17p13.3 microduplication syn... - 8g21 (2,041 bytes)
9: ...://www.uniprot.org/uniprot/RELN_HUMAN RELN_HUMAN] Lissencephaly syndrome, Norman-Roberts type;Autosomal dominant ... - 8oi8 (3,052 bytes)
11: ...n malformation consisting of anterior-predominant lissencephaly. Other typical features include postnatal short s... - 8sh7 (2,135 bytes)
11: .../www.uniprot.org/uniprot/TBA1A_HUMAN TBA1A_HUMAN] Lissencephaly due to TUBA1A mutation. The disease is caused by ... - 8ptk (4,385 bytes)
11: ...ller-Dieker syndrome;Subcortical band heterotopia;Lissencephaly due to LIS1 mutation;17p13.3 microduplication syn... - 5ip4 (6,525 bytes)
10: ... chromosomal aberration involving DCX is found in lissencephaly. Translocation t(X;2)(q22.3;p25.1). - 5in7 (6,442 bytes)
10: ... chromosomal aberration involving DCX is found in lissencephaly. Translocation t(X;2)(q22.3;p25.1). - 5io9 (6,441 bytes)
10: ... chromosomal aberration involving DCX is found in lissencephaly. Translocation t(X;2)(q22.3;p25.1).
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