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1.
FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome.
Expert Rev Mol Med
; 19: e10, 2017 07 19.
Article
in English
| MEDLINE | ID: mdl-28720156
2.
Identification of novel microsatellite markers <1 Mb from the HBB gene and development of a single-tube pentadecaplex PCR panel of highly polymorphic markers for preimplantation genetic diagnosis of beta-thalassemia.
Electrophoresis
; 36(23): 2914-24, 2015 Dec.
Article
in English
| MEDLINE | ID: mdl-26331357
3.
Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome.
Prenat Diagn
; 35(6): 534-43, 2015 Jun.
Article
in English
| MEDLINE | ID: mdl-25641621
4.
The FGF and FGFR Gene Family and Risk of Cleft Lip With or Without Cleft Palate.
Cleft Palate Craniofac J
; 50(1): 96-103, 2013 Jan.
Article
in English
| MEDLINE | ID: mdl-22074045
5.
Simultaneous Screening of the FRAXA and FRAXE Loci for Rapid Detection of FMR1 CGG and/or AFF2 CCG Repeat Expansions by Triplet-Primed PCR.
J Mol Diagn
; 23(8): 941-951, 2021 08.
Article
in English
| MEDLINE | ID: mdl-34111553
6.
Rapid and reliable preimplantation genetic diagnosis of common hemoglobin Bart's hydrops fetalis syndrome and hemoglobin H disease determinants using an enhanced single-tube decaplex polymerase chain reaction assay.
Am J Hematol
; 90(9): E194-6, 2015 Sep.
Article
in English
| MEDLINE | ID: mdl-26043722
7.
Phylogenetic and evolutionary relationships and developmental expression patterns of the zebrafish twist gene family.
Dev Genes Evol
; 219(6): 289-300, 2009 Jun.
Article
in English
| MEDLINE | ID: mdl-19565261
8.
Identification of Novel Microsatellite Markers Flanking the SMN1 and SMN2 Duplicated Region and Inclusion Into a Single-Tube Tridecaplex Panel for Haplotype-Based Preimplantation Genetic Testing of Spinal Muscular Atrophy.
Front Genet
; 10: 1105, 2019.
Article
in English
| MEDLINE | ID: mdl-31781167
9.
Improved high sensitivity screen for Huntington disease using a one-step triplet-primed PCR and melting curve assay.
PLoS One
; 12(7): e0180984, 2017.
Article
in English
| MEDLINE | ID: mdl-28700716
10.
Fetal polymorphisms at the ABCB1-transporter gene locus are associated with susceptibility to non-syndromic oral cleft malformations.
Eur J Hum Genet
; 21(12): 1436-41, 2013 Dec.
Article
in English
| MEDLINE | ID: mdl-23443032
11.
BMP4 was associated with NSCL/P in an Asian population.
PLoS One
; 7(4): e35347, 2012.
Article
in English
| MEDLINE | ID: mdl-22514733
12.
Tgfbeta3 regulation of chondrogenesis and osteogenesis in zebrafish is mediated through formation and survival of a subpopulation of the cranial neural crest.
Mech Dev
; 127(7-8): 329-44, 2010.
Article
in English
| MEDLINE | ID: mdl-20406684
13.
Germline transgenesis of zebrafish using the medaka Tol1 transposon system.
Dev Dyn
; 237(9): 2466-74, 2008 Sep.
Article
in English
| MEDLINE | ID: mdl-18729212
14.
Zebrafish twist1 is expressed in craniofacial, vertebral, and renal precursors.
Dev Genes Evol
; 217(11-12): 783-9, 2007 Dec.
Article
in English
| MEDLINE | ID: mdl-17929053
15.
Genomic, cDNA, and embryonic expression analysis of zebrafish transforming growth factor beta 3 (tgfbeta3).
Dev Dyn
; 232(4): 1021-30, 2005 Apr.
Article
in English
| MEDLINE | ID: mdl-15739231
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