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26 NOTCH2 MUTATIONS IN ALAGILLE SYNDROME
by
Kamath, B.M
,
Hutchinson, A
,
Bauer, R
,
Gerfen, J
,
Krantz, I.D
,
Piccoli, D.A
,
Spinner, N.B
,
Loomes, K.M
Published in
Journal of hepatology
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Monosomy 1p36 uncovers a role for OX40 in survival of activated CD4+ T cells
by
Suhoski, M.M
,
Perez, E.E
,
Heltzer, M.L
,
Laney, A
,
Shaffer, L.G
,
Saitta, S
,
Nachman, S
,
Spinner, N.B
,
June, C.H
,
Orange, J.S
Published in
Clinical immunology (Orlando, Fla.)
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Consequences of JAG1 mutations
by
Kamath, B M
,
Bason, L
,
Piccoli, D A
,
Krantz, I D
,
Spinner, N B
Published in
Journal of medical genetics
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Cytologically balanced t(2;20) in a two-generation family with Alagille syndrome : cytogenetic and molecular studies
by
SPINNER, N. B
,
RAND, E. B
,
FORTINA, P
,
GENIN, A
,
TAUB, R
,
SEMERARO, A
,
PICCOLI, D. A
Published in
American journal of human genetics
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American Journal Of Human Genetics
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