|
π
|
Alleles of the APC gene: An attenuated form of familial polyposis
19 auth.
L. Spirio,
S. Olschwang,
J. Groden,
M. Robertson,
W. Samowitz,
G. Joslyn,
L. Gelbert,
A. Thliveris,
M. Carlson,
B. Otterud,
...
H. Lynch,
P. Watson,
P. Lynch,
P. Laurent-Puig,
R. Burt,
J. P. Hughes,
G. Thomas,
M. Leppert,
Raymond White
|
9 |
1993 |
9
π
|
|
π
|
Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia.
10 auth.
B. Bejjani,
R. Lewis,
K. Tomey,
K. Anderson,
D. Dueker,
M. Jabak,
...
W. Astle,
B. Otterud,
M. Leppert,
J. Lupski
|
8 |
1998 |
8
π
|
|
π
|
Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1.
8 auth.
K. Flanigan,
Kathy L. Gardner,
K. Alderson,
B. Galster,
B. Otterud,
M. Leppert,
...
C. Kaplan,
L. PtΓ‘Δek
|
7 |
1996 |
7
π
|
|
π
|
A locus for febrile seizures (FEB3) maps to chromosome 2q23β24
10 auth.
A. Peiffer,
J. Thompson,
Carole Charlier,
B. Otterud,
T. Varvil,
C. Pappas,
...
Craig Barnitz,
Kristen M. Gruenthal,
RenΓ©e Kuhn,
M. Leppert
|
7 |
1999 |
7
π
|
|
π
|
Linkage of a variant or attenuated form of adenomatous polyposis coli to the adenomatous polyposis coli (APC) locus.
13 auth.
L. Spirio,
B. Otterud,
D. Stauffer,
H. Lynch,
P. Lynch,
P. Watson,
S. Lanspa,
T. Smyrk,
J. Cavalieri,
Linda Howard,
...
R. Burt,
Raymond White,
M. Leppert
|
7 |
1992 |
7
π
|
|
π
|
Genetic mapping of ossification of the posterior longitudinal ligament of the spine.
11 auth.
H. Koga,
T. Sakou,
E. Taketomi,
Kyouji Hayashi,
Takuya Numasawa,
S. Harata,
...
K. Yone,
S. Matsunaga,
B. Otterud,
I. Inoue,
M. Leppert
|
7 |
1998 |
7
π
|
|
π
|
Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q.
10 auth.
K. Fink,
'. C. B. Wu,
M. Jones,
'. G. B. Sharp,
B. Lange,
A. Lesicki,
...
T. Reinglass,
'. T. Varvil,
B. Otterud,
M. Leppert
|
7 |
1995 |
7
π
|
|
π¬
|
Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity.
rd H Heath,
C. Jackson,
B. Otterud,
M. Leppert
|
7 |
1993 |
7
π¬
|
|
π
|
Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22.1.
12 auth.
Charles A. Klanke,
Yan Ru Su,
D. F. Callen,
Zhuo Wang,
Pierre Meneton,
Nancy Baird,
...
Ramani A. Kandasamy,
John Orlowski,
B. Otterud,
M. Leppert,
G. Shull,
Anil G. Menon
|
7 |
1995 |
7
π
|
|
π
|
Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p
9 auth.
D. Drayna,
H. Coon,
U. Kim,
T. Elsner,
K. Cromer,
B. Otterud,
...
L. Baird,
A. Peiffer,
M. Leppert
|
7 |
2003 |
7
π
|
|
π
|
Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q.
9 auth.
R. A. Lewis,
B. Otterud,
B. Otterud,
Dora Stauffer,
Dora Stauffer,
J. Lalouel,
...
J. Lalouel,
M. Leppert,
M. Leppert
|
7 |
1990 |
7
π
|
