Search details
1.
Pluripotent Stem Cells in Clinical Setting-New Developments and Overview of Current Status.
Stem Cells
; 40(9): 791-801, 2022 09 26.
Article
in English
| MEDLINE | ID: mdl-35671338
2.
Effects of thyroid hormone on mitochondria and metabolism of human preimplantation embryos.
Stem Cells
; 38(3): 369-381, 2020 03.
Article
in English
| MEDLINE | ID: mdl-31778245
3.
A novel non-invasive prenatal sickle cell disease test for all at-risk pregnancies.
Br J Haematol
; 190(1): 119-124, 2020 07.
Article
in English
| MEDLINE | ID: mdl-32097993
4.
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.
PLoS Genet
; 12(5): e1005993, 2016 05.
Article
in English
| MEDLINE | ID: mdl-27153221
5.
Concise Review: Human Embryonic Stem Cells-What Have We Done? What Are We Doing? Where Are We Going?
Stem Cells
; 35(1): 17-25, 2017 01.
Article
in English
| MEDLINE | ID: mdl-27350255
6.
Microduplications at the pseudoautosomal SHOX locus in autism spectrum disorders and related neurodevelopmental conditions.
J Med Genet
; 53(8): 536-47, 2016 08.
Article
in English
| MEDLINE | ID: mdl-27073233
7.
Gestation related karyotype, QF-PCR and CGH-array failure rates in diagnostic amniocentesis.
Prenat Diagn
; 36(8): 708-13, 2016 Aug.
Article
in English
| MEDLINE | ID: mdl-27192044
8.
Autism and chromosome abnormalities-A review.
Clin Anat
; 29(5): 620-7, 2016 Jul.
Article
in English
| MEDLINE | ID: mdl-27012322
9.
Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation.
Hum Mutat
; 36(9): 842-50, 2015 Sep.
Article
in English
| MEDLINE | ID: mdl-26010655
10.
Rare deletions at the neurexin 3 locus in autism spectrum disorder.
Am J Hum Genet
; 90(1): 133-41, 2012 Jan 13.
Article
in English
| MEDLINE | ID: mdl-22209245
11.
Developmental clock compromises human twin model created by embryo splitting.
Hum Reprod
; 30(12): 2774-84, 2015 Dec.
Article
in English
| MEDLINE | ID: mdl-26489438
12.
Phenotypic features in patients with 15q11.2(BP1-BP2) deletion: further delineation of an emerging syndrome.
Am J Med Genet A
; 164A(8): 1916-22, 2014 Aug.
Article
in English
| MEDLINE | ID: mdl-24715682
13.
Deficiency of the cyclin-dependent kinase inhibitor, CDKN1B, results in overgrowth and neurodevelopmental delay.
Hum Mutat
; 34(6): 864-8, 2013 Jun.
Article
in English
| MEDLINE | ID: mdl-23505216
14.
Successful PGD cycles for mosaic Robertsonian translocation carriers provide insights into the mechanism of formation of the derivative chromosomes.
Am J Med Genet A
; 161A(3): 566-71, 2013 Mar.
Article
in English
| MEDLINE | ID: mdl-23401053
15.
Multiple pregnancy, fetal reduction and selective termination.
Reprod Biomed Online
; 26(6): 522-4, 2013 Jun.
Article
in English
| MEDLINE | ID: mdl-23602677
16.
Care needed in interpretation of chromosome rearrangements.
Reprod Biomed Online
; 37(5): 651, 2018 11.
Article
in English
| MEDLINE | ID: mdl-30385143
17.
Embryo selection in IVF: is polar body array comparative genomic hybridization accurate enough?
Hum Reprod
; 27(4): 951-3, 2012 Apr.
Article
in English
| MEDLINE | ID: mdl-22328558
18.
Derivation and feeder-free propagation of human embryonic stem cells under xeno-free conditions.
Cytotherapy
; 14(1): 122-8, 2012 Jan.
Article
in English
| MEDLINE | ID: mdl-22029654
19.
QF-PCR: application, overview and review of the literature.
Prenat Diagn
; 32(4): 309-14, 2012 Apr.
Article
in English
| MEDLINE | ID: mdl-22467160
20.
Quantitative fluorescence PCR analysis of >40,000 prenatal samples for the rapid diagnosis of trisomies 13, 18 and 21 and monosomy X.
Prenat Diagn
; 32(12): 1197-204, 2012 Dec.
Article
in English
| MEDLINE | ID: mdl-23097180