Detalhe da pesquisa
1.
The clinical utility of PGD with HLA matching: a collaborative multi-centre ESHRE study.
Hum Reprod
; 33(3): 520-530, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29432583
2.
Clinical and molecular consequences of disease-associated de novo mutations in SATB2.
Genet Med
; 19(8): 900-908, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28151491
3.
One-cell biopsy significantly improves the outcome of preimplantation genetic diagnosis (PGD) treatment: retrospective analysis of 569 PGD cycles at the Stockholm PGD centre.
Hum Reprod
; 27(9): 2843-9, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22736325
4.
High white matter lesion load is associated with hippocampal atrophy in mild cognitive impairment.
Dement Geriatr Cogn Disord
; 31(2): 132-8, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21293123
5.
Improved structural characterization of chromosomal breakpoints using high resolution custom array-CGH.
Clin Genet
; 77(6): 552-62, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20236111
6.
Detailed molecular and clinical characterization of three patients with 21q deletions.
Clin Genet
; 77(2): 145-54, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19863549
7.
Combination of hippocampal volume and cerebrospinal fluid biomarkers improves predictive value in mild cognitive impairment.
Dement Geriatr Cogn Disord
; 29(4): 294-300, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20389071
8.
Padlock probes: circularizing oligonucleotides for localized DNA detection.
Science
; 265(5181): 2085-8, 1994 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-7522346
9.
Concurrent microdeletion and duplication of 22q11.2.
Clin Genet
; 74(1): 61-7, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18445048
10.
Small baseline volume of left hippocampus is associated with subsequent conversion of MCI into dementia: the Göteborg MCI study.
J Neurol Sci
; 272(1-2): 48-59, 2008 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18571674
11.
Detecting Genes with Ligases
Methods
; 9(1): 84-90, 1996 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-9245346
12.
Presence of an IDS-related locus (IDS2) in Xq28 complicates the mutational analysis of Hunter syndrome.
Eur J Hum Genet
; 3(4): 219-27, 1995.
Artigo
em Inglês
| MEDLINE | ID: mdl-8528670
13.
Strong founder effect for the fragile X syndrome in Sweden.
Eur J Hum Genet
; 2(2): 103-9, 1994.
Artigo
em Inglês
| MEDLINE | ID: mdl-8044655
14.
New X-linked syndrome with severe mental retardation, severely impaired vision, severe hearing defect, epileptic seizures, spasticity, restricted joint mobility, and early death.
Am J Med Genet
; 45(5): 654-8, 1993 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-8456840
15.
Infantile autism--fragile X: molecular findings support genetic heterogeneity.
Am J Med Genet
; 44(6): 830-3, 1992 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-1481857
16.
Carrier detection of the fragile X syndrome using flanking loci DXS98, DXS105, and DXS304.
Am J Med Genet
; 38(2-3): 319-21, 1991.
Artigo
em Inglês
| MEDLINE | ID: mdl-1673304
17.
Methylation and mutation patterns in the fragile X syndrome.
Am J Med Genet
; 43(1-2): 268-78, 1992.
Artigo
em Inglês
| MEDLINE | ID: mdl-1605200
18.
Pharmacokinetics of dipotassium chlorazepate in patients after repeated 50 mg oral doses.
Psychopharmacology (Berl)
; 71(2): 165-7, 1980.
Artigo
em Inglês
| MEDLINE | ID: mdl-6108593
19.
Comparison studies of chlorazepate administered as a divided daily dose and as a single dose at night.
Psychopharmacology (Berl)
; 57(2): 123-6, 1978 Apr 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-26099
20.
Pharmacokinetics of N-desmethyldiazepam in healthy volunteers after single daily doses of dipotassium chlorazepate.
Psychopharmacology (Berl)
; 53(2): 105-9, 1977 Jul 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-19801