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Results of search for 'au:"Cram, David S"', page 1 of 3
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Cram, David S
Fan, Junmei
Jones, Gayle M
Li, Huanzheng
Li, Na
Li, Zhifeng
Liang, Desheng
Liu, Juntao
Liu, Yiqian
Ma, Minyue
Qi, Qingwei
Song, Bi
Song, Zhuo
Trounson, Alan O
Wang, Hui
Wang, Li
Xu, Genming
Xu, Mengnan
Yao, Yuanqing
Zhang, Jianguang
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Adult
Aneuploidy
Chromosome Aberrations
Chromosome Disorders
DNA
DNA Copy Number Variations
Female
Genetic Testing
High-Throughput Nucleotide Sequencing
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Karyotyping
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Pregnancy
Preimplantation Diagnosis
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1.
Potential of syncytiotrophoblasts isolated from the cervical mucus for early non-invasive prenatal diagnosis: evidence of a vanishing twin.
[electronic resource]
by
Mantzaris, Debbie
Cram, David S
Producer:
20150720
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 438
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2.
Next generation sequencing: Coping with rare genetic diseases in China.
[electronic resource]
by
Cram, David S
Zhou, Daixing
Producer:
20160927
In:
Intractable & rare diseases research
vol. 5
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3.
Genotyping of Rhesus SCNT pluripotent stem cell lines.
[electronic resource]
by
Cram, David S
Song, Bi
Trounson, Alan O
Producer:
20071220
In:
Nature
vol. 450
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4.
Y chromosome microdeletions: implications for assisted conception.
[electronic resource]
by
Cram, David S
Osborne, Elissa
McLachlan, Robert I
Producer:
20070109
In:
The Medical journal of Australia
vol. 185
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5.
Feasibility of noninvasive prenatal testing for common fetal aneuploidies in an early gestational window.
[electronic resource]
by
Shi, Xiaolin
Zhang, Zhitao
Cram, David S
Liu, Caixia
Producer:
20150826
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 439
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6.
DNA identification of fetal cells isolated from cervical mucus: potential for early non-invasive prenatal diagnosis.
[electronic resource]
by
Katz-Jaffe, Mandy G
Mantzaris, Debbie
Cram, David S
Producer:
20050614
In:
BJOG : an international journal of obstetrics and gynaecology
vol. 112
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7.
Chromosome 21 mosaic human preimplantation embryos predominantly arise from diploid conceptions.
[electronic resource]
by
Katz-Jaffe, Mandy G
Trounson, Alan O
Cram, David S
Producer:
20051227
In:
Fertility and sterility
vol. 84
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8.
The Beta-amyloid protein of Alzheimer's disease: communication breakdown by modifying the neuronal cytoskeleton.
[electronic resource]
by
Mokhtar, Sara H
Bakhuraysah, Maha M
Cram, David S
Petratos, Steven
Producer:
20140624
In:
International journal of Alzheimer's disease
vol. 2013
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9.
Optimization of a microarray based approach for deriving representative gene expression profiles from human oocytes.
[electronic resource]
by
Jones, Gayle M
Song, Bi
Cram, David S
Trounson, Alan O
Producer:
20070124
In:
Molecular reproduction and development
vol. 74
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10.
Issues and concerns of couples presenting for preimplantation genetic diagnosis (PGD).
[electronic resource]
by
Katz, Mandy G
Fitzgerald, Lara
Bankier, Agnes
Savulescu, Julian
Cram, David S
Producer:
20030520
In:
Prenatal diagnosis
vol. 22
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11.
Birth of a child with trisomy 9 mosaicism syndrome associated with paternal isodisomy 9: case of a positive noninvasive prenatal test result unconfirmed by invasive prenatal diagnosis.
[electronic resource]
by
Ma, Jingmei
Cram, David S
Zhang, Jianguang
Shang, Ling
Yang, Huixia
Pan, Hong
Producer:
20150629
In:
Molecular cytogenetics
vol. 8
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12.
Novel strategy with potential to identify developmentally competent IVF blastocysts.
[electronic resource]
by
Jones, Gayle M
Cram, David S
Song, Bi
Kokkali, Georgia
Pantos, Kostas
Trounson, Alan O
Producer:
20080929
In:
Human reproduction (Oxford, England)
vol. 23
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13.
Maternal X chromosome copy number variations are associated with discordant fetal sex chromosome aneuploidies detected by noninvasive prenatal testing.
[electronic resource]
by
Wang, Shaowei
Huang, Shuai
Ma, Linlin
Liang, Lin
Zhang, Junrong
Zhang, Jianguang
Cram, David S
Producer:
20160304
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 444
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14.
Mesenchymal stem cells for treatment of CNS injury.
[electronic resource]
by
Azari, Michael F
Mathias, Louisa
Ozturk, Ezgi
Cram, David S
Boyd, Richard L
Petratos, Steven
Producer:
20110714
In:
Current neuropharmacology
vol. 8
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15.
Characterization of forebrain neurons derived from late-onset Huntington's disease human embryonic stem cell lines.
[electronic resource]
by
Niclis, Jonathan C
Pinar, Anita
Haynes, John M
Alsanie, Walaa
Jenny, Robert
Dottori, Mirella
Cram, David S
Producer:
20130412
In:
Frontiers in cellular neuroscience
vol. 7
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16.
A novel MSX1 intronic mutation associated with autosomal dominant non-syndromic oligodontia in a large Chinese family pedigree.
[electronic resource]
by
Xue, Jinjie
Gao, Qingping
Huang, Yanru
Zhang, Xiaoyu
Yang, Pu
Cram, David S
Liang, Desheng
Wu, Lingqian
Producer:
20170206
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 461
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17.
A comparative study of EGFR oncogenic mutations in matching tissue and plasma samples from patients with advanced non-small cell lung carcinoma.
[electronic resource]
by
Chai, Xiaofei
Ren, Pengfei
Wei, Bing
Ma, Jie
Mai, Ling
Cram, David S
Song, Yongping
Guo, Yongjun
Producer:
20170217
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 457
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18.
Placental Up-Regulation of Leptin and ARMS2 is Associated with Growth Discordance in Monochorionic Diamniotic Twin Pregnancies.
[electronic resource]
by
Sun, Luming
Zhou, Jia
Wang, Kai
Wang, Jian
Shang, Ling
Zhang, Jianguang
Wu, Junqing
Cram, David S
Producer:
20171208
In:
Twin research and human genetics : the official journal of the International Society for Twin Studies
vol. 20
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19.
Monochorionic twins with unequal placental sharing: why can the outcome still be favorable?
[electronic resource]
by
Sun, Lu-Ming
Li, Ying
Zou, Gang
Zhou, Fenghe
Lei, Xiaoping
Cram, David S
Oepkes, Dick
Wu, Junqing
Producer:
20161019
In:
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians
vol. 29
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20.
Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencing.
[electronic resource]
by
Zhu, Xiangyu
Li, Jie
Ru, Tong
Wang, Yaping
Xu, Yan
Yang, Ying
Wu, Xing
Cram, David S
Hu, Yali
Producer:
20170113
In:
Prenatal diagnosis
vol. 36
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