相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Feasibility of DNA diagnosis of haemoglobinopathies on coelocentesis
Antonino Giambona et al.
BRITISH JOURNAL OF HAEMATOLOGY (2011)
Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post-array CGH era?
The-Hung Bui et al.
PRENATAL DIAGNOSIS (2011)
Whole genome amplification and real-time PCR in forensic casework
Emiliano Giardina et al.
BMC GENOMICS (2009)
Acrania/encephalocele sequence (exencephaly) associated with 92,XXXX karyotype: Early prenatal diagnosis at 9+5weeks by 3D transvaginal ultrasound and coelocentesis
Gabriele Tonni et al.
CONGENITAL ANOMALIES (2009)
Coelomic fluid analysis: the absolute necessity to prove its fetal origin
Jean-Marie Jouannic et al.
REPRODUCTIVE BIOMEDICINE ONLINE (2008)
Effect of high throughput RHD typing of fetal DNA in maternal plasma on use of anti-RhD immunoglobulin in RhD negative pregnant women:: prospective feasibility study
Kirstin Finning et al.
BRITISH MEDICAL JOURNAL (2008)
Innovation - Prenatal diagnosis: progress through plasma nucleic acids
Y. M. Dennis Lo et al.
NATURE REVIEWS GENETICS (2007)
Whole genome amplification from a single cell: a new era for preimplantation genetic diagnosis
Serdar Coskun et al.
PRENATAL DIAGNOSIS (2007)
Detection of low-level mosaicism by array CGH in routine diagnostic specimens
Blake C. Balliff et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2006)
Very early prenatal diagnosis of genetic diseases based on coelomic fluid analysis:: a feasibility study
Jean-Marie Jouannic et al.
HUMAN REPRODUCTION (2006)
Aneuploidy screening in coelomic samples using fluorescence in situ hybridisation (FISH)
K Chatzimeletiou et al.
PRENATAL DIAGNOSIS (2005)
Early prenatal diagnosis by celocentesis
G Makrydimas et al.
ULTRASOUND IN OBSTETRICS & GYNECOLOGY (2004)
New strategy for prenatal diagnosis of X-linked disorders.
JM Costa et al.
NEW ENGLAND JOURNAL OF MEDICINE (2002)