-
1
-
-
0025137740
-
Neuropsychological, neurological and neuroanatomical profile of Williams syndrome
-
U Bellugi A Bihrle T Jernigan D Trauner S Doherty Neuropsychological, neurological and neuroanatomical profile of Williams syndrome Am J Med Genet 6 1990 115 125
-
(1990)
Am J Med Genet
, vol.6
, pp. 115-125
-
-
Bellugi, U1
Bihrle, A2
Jernigan, T3
Trauner, D4
Doherty, S5
-
2
-
-
0026778460
-
Syntaxin: a synaptic protein implicated in docking of synaptic vesicles at presynaptic active zones
-
MK Bennett N Calakos RH Scheller Syntaxin: a synaptic protein implicated in docking of synaptic vesicles at presynaptic active zones Science 257 1992 255 259
-
(1992)
Science
, vol.257
, pp. 255-259
-
-
Bennett, MK1
Calakos, N2
Scheller, RH3
-
3
-
-
0025022133
-
Hypothesis for development of a behavioral phenotype in Williams syndrome
-
CV Dilts CA Morris CO Leonard Hypothesis for development of a behavioral phenotype in Williams syndrome Am J Med Genet Suppl 6 1990 126 131
-
(1990)
Am J Med Genet Suppl
, vol.6
, pp. 126-131
-
-
Dilts, CV1
Morris, CA2
Leonard, CO3
-
4
-
-
0027185655
-
Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome
-
AK Ewart CA Morris D Atkinson W Jin K Sternes P Spallone AD Stock Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome Nat Genet 5 1993 11 16
-
(1993)
Nat Genet
, vol.5
, pp. 11-16
-
-
Ewart, AK1
Morris, CA2
Atkinson, D3
Jin, W4
Sternes, K5
Spallone, P6
Stock, AD7
-
7
-
-
0025070995
-
Williams syndrome professional symposium
-
F Greenberg Williams syndrome professional symposium Am J Med Genet Suppl 6 1990 85 88
-
(1990)
Am J Med Genet Suppl
, vol.6
, pp. 85-88
-
-
Greenberg, F1
-
8
-
-
0029947330
-
Mouse model of hyperkinesis implicates SNAP-25 in behavioural regulation
-
EJ Hess KA Collins MC Wilson Mouse model of hyperkinesis implicates SNAP-25 in behavioural regulation J Neurosci 16 1996 3104 3111
-
(1996)
J Neurosci
, vol.16
, pp. 3104-3111
-
-
Hess, EJ1
Collins, KA2
Wilson, MC3
-
9
-
-
0026642183
-
Spontaneous locomotor hyperactivity in a mouse mutant with a deletion including the Snap gene on chromosome 2
-
EJ Hess HA Jinnah CA Kozak MC Wilson Spontaneous locomotor hyperactivity in a mouse mutant with a deletion including the Snap gene on chromosome 2 J Neurosci 12 1992 2865 2874
-
(1992)
J Neurosci
, vol.12
, pp. 2865-2874
-
-
Hess, EJ1
Jinnah, HA2
Kozak, CA3
Wilson, MC4
-
11
-
-
0027366004
-
Williams syndrome: autosomal dominant inheritance
-
CA Morris IT Thomas F Greenberg Williams syndrome: autosomal dominant inheritance Am J Med Genet 47 1993 478 481
-
(1993)
Am J Med Genet
, vol.47
, pp. 478-481
-
-
Morris, CA1
Thomas, IT2
Greenberg, F3
-
12
-
-
0028905182
-
Deletions of the elastin gene at 7q11.23 occur in ~90% of patients with Williams syndrome
-
E Nickerson F Greenberg MT Keating C McCaskill LG Shaffer Deletions of the elastin gene at 7q11.23 occur in ~90% of patients with Williams syndrome Am J Hum Genet 56 1995 1156 1161
-
(1995)
Am J Hum Genet
, vol.56
, pp. 1156-1161
-
-
Nickerson, E1
Greenberg, F2
Keating, MT3
McCaskill, C4
Shaffer, LG5
-
13
-
-
0030249984
-
Identification of genes from a 500 kb region at 7q11.23 that is commonly deleted in Williams syndrome
-
LR Osborne D Martindale SW Scherer X-M Shi J Huizenga HQ Heng T Costa Identification of genes from a 500 kb region at 7q11.23 that is commonly deleted in Williams syndrome Genomics 36 1996 328 336
-
(1996)
Genomics
, vol.36
, pp. 328-336
-
-
Osborne, LR1
Martindale, D2
Scherer, SW3
Shi, X-M4
Huizenga, J5
Heng, HQ6
Costa, T7
-
14
-
-
0029948577
-
The gene for replication factor C subunit 2 (RFC2) is within the 7q11.23 Williams syndrome deletion
-
R Peoples L Perez-Jurado Y-K Wang P Kaplan U Francke The gene for replication factor C subunit 2 (RFC2) is within the 7q11.23 Williams syndrome deletion Am J Hum Genet 58 1996 1370 1373
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1370-1373
-
-
Peoples, R1
Perez-Jurado, L2
Wang, Y-K3
Kaplan, P4
Francke, U5
-
15
-
-
0029805704
-
Williams syndrome: an overview of medical, cognitive, and behavioral features
-
BR Pober EM Dykens Williams syndrome: an overview of medical, cognitive, and behavioral features Child Adolesc Psychiatr Clin North Am 5 1996 929 943
-
(1996)
Child Adolesc Psychiatr Clin North Am
, vol.5
, pp. 929-943
-
-
Pober, BR1
Dykens, EM2
-
17
-
-
0027429044
-
The Williams syndrome: evidence for possible autosomal dominant inheritance
-
LS Sadler LK Robinson KR Verdaasdonk R Gingell The Williams syndrome: evidence for possible autosomal dominant inheritance Am J Med Genet 47 1993 486 470
-
(1993)
Am J Med Genet
, vol.47
, pp. 486
-
-
Sadler, LS1
Robinson, LK2
Verdaasdonk, KR3
Gingell, R4
-
18
-
-
0028817584
-
Genetic and electrophysiological studies of Drosophila syntaxin-1A demonstrate its role in nonneuronal secretion and neuro-transmission
-
KL Schulze K Broadie MS Perin HJ Bellen Genetic and electrophysiological studies of Drosophila syntaxin-1A demonstrate its role in nonneuronal secretion and neuro-transmission Cell 80 1995 311 320
-
(1995)
Cell
, vol.80
, pp. 311-320
-
-
Schulze, KL1
Broadie, K2
Perin, MS3
Bellen, HJ4
-
19
-
-
0030048838
-
Calcium-dependent interaction of N-type calcium channels with the synaptic core complex
-
Z-H Sheng J Rettig T Cook WA Catterall Calcium-dependent interaction of N-type calcium channels with the synaptic core complex Nature 379 1996 451 454
-
(1996)
Nature
, vol.379
, pp. 451-454
-
-
Sheng, Z-H1
Rettig, J2
Cook, T3
Catterall, WA4
-
21
-
-
0031043863
-
A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome delrtion at 7q11.23
-
YK Wang CH Samos R Peoples LA Perez-Jurado R Nusse U Francke A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome delrtion at 7q11.23 Hum Mol Genet 6 1997 465 472
-
(1997)
Hum Mol Genet
, vol.6
, pp. 465-472
-
-
Wang, YK1
Samos, CH2
Peoples, R3
Perez-Jurado, LA4
Nusse, R5
Francke, U6
-
22
-
-
0029021036
-
Cloning and sequence analysis of a cDNA encoding human syntaxin 1A, a polypeptide essential for exocytosis
-
R Zhang AB Maksymowych LL Simpson Cloning and sequence analysis of a cDNA encoding human syntaxin 1A, a polypeptide essential for exocytosis Gene 159 1995 293 294
-
(1995)
Gene
, vol.159
, pp. 293-294
-
-
Zhang, R1
Maksymowych, AB2
Simpson, LL3
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