Found: 30
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Preimplantation genetic diagnosis of inherited cancer: Familial adenomatous polyposis coli.
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- Journal of Assisted Reproduction & Genetics, 1998, v. 15, n. 3, p. 140, doi. 10.1023/A:1023008921386
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- Article
Prospect of preimplantation genetic diagnosis for heritable mitochondrial DNA diseases.
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- Molecular Human Reproduction, 2004, v. 10, n. 8, p. 621, doi. 10.1093/molehr/gah085
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- Article
Prospect of preimplantation genetic diagnosis for heritable mitochondrial DNA diseases.
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- Molecular Human Reproduction, 2003, v. 9, n. 10, p. 631, doi. 10.1093/molehr/gag077
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- Article
Assessment of multiplex fluorescent PCR for screening single cells for trisomy 21 and single gene defects.
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- Molecular Human Reproduction, 1999, v. 5, n. 12, p. 1166, doi. 10.1093/molehr/5.12.1166
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- Article
Outcomes of Preimplantation Genetic Testing for Single Gene Defects in a Privately Funded Period and Publicly Funded Period: A North-American Single Center Experience.
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- Journal of Reproduction & Infertility, 2020, v. 21, n. 2, p. 107
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- Publication type:
- Article
Paternal transcripts for glucose-6-phosphate dehydrogenase and adenosine deaminase are first detectable in the human preimplantation embryo at the Three- to Four-Cell stage.
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- Molecular Reproduction & Development, 1997, v. 48, n. 4, p. 442, doi. 10.1002/(SICI)1098-2795(199712)48:4<442::AID-MRD4>3.0.CO;2-Q
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- Article
Transcription of circular and noncircular forms of Sry in mouse testes.
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- Molecular Reproduction & Development, 1994, v. 37, n. 4, p. 370, doi. 10.1002/mrd.1080370403
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- Article
Sites of transcription of the Müllerian inhibiting substance gene in mouse testis.
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- Molecular Reproduction & Development, 1993, v. 35, n. 2, p. 159, doi. 10.1002/mrd.1080350209
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- Article
Gene expression, X-inactivation, and methylation during spermatogenesis: The case of Zfa, Zfx, and Zfy in mice.
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- Molecular Reproduction & Development, 1993, v. 35, n. 2, p. 114, doi. 10.1002/mrd.1080350203
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- Article
Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.
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- Nature Genetics, 2006, v. 38, n. 3, p. 300, doi. 10.1038/ng1740
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- Article
Successful preimplantation genetic diagnosis for sex linked Lesch-Nyhan syndrome using specific diagnosis.
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- Prenatal Diagnosis, 1999, v. 19, n. 13, p. 1237, doi. 10.1002/(SICI)1097-0223(199912)19:13<1237::AID-PD726>3.0.CO;2-O
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- Article
Assessment of the reliability of single blastomere analysis for preimplantation diagnosis of the ΔF508 deletion causing cystic fibrosis in clinical practice.
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- Prenatal Diagnosis, 1998, v. 18, n. 13, p. 1402, doi. 10.1002/(SICI)1097-0223(199812)18:13<1402::AID-PD500>3.0.CO;2-T
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- Publication type:
- Article
CLINICAL EXPERIENCE WITH PREIMPLANTATION GENETIC DIAGNOSIS OF CYSTIC FIBROSIS (ΔF508).
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- Prenatal Diagnosis, 1996, v. 16, n. 2, p. 137, doi. 10.1002/(SICI)1097-0223(199602)16:2<137::AID-PD824>3.0.CO;2-H
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- Publication type:
- Article
Chromosome Segregation Analysis in Human Embryos Obtained from Couples Involving Male Carriers of Reciprocal or Robertsonian Translocation.
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- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0046046
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- Article
Vasoactive Intestinal Peptide and Its Receptors in Human Ovarian Cortical Follicles.
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- PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0037015
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- Article
Report of four new patients with protein-truncating mutations in C6orf221/KHDC3L and colocalization with NLRP7.
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- European Journal of Human Genetics, 2013, v. 21, n. 9, p. 957, doi. 10.1038/ejhg.2012.274
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- Article
Transmission ratio distortion in the myotonic dystrophy locus in human preimplantation embryos.
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- European Journal of Human Genetics, 2006, v. 14, n. 3, p. 299, doi. 10.1038/sj.ejhg.5201559
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- Article
NLRP7 and KHDC3L, the two maternal-effect proteins responsible for recurrent hydatidiform moles, co-localize to the oocyte cytoskeleton.
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- Human Reproduction, 2015, v. 30, n. 1, p. 159, doi. 10.1093/humrep/deu291
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- Article
Transcription of paternal Y-linked genes in the human zygote as early as the pronucleate stage.
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- Zygote, 1994, v. 2, n. 4, p. 281, doi. 10.1017/S0967199400002100
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- Article
Chromosomal mosaicism throughout human preimplantation development in vitro: incidence, type, and relevance to embryo outcome.
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- 2002
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- Publication type:
- journal article
Genetics and genetic diagnosis. Fluorescence in-situ hybridization of sex chromosomes in spermatozoa and spare preimplantation embryos of a Klinefelter 46,XY/47,XXY male.
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- Human Reproduction, 2000, v. 15, n. 2, p. 440, doi. 10.1093/humrep/15.2.440
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- Publication type:
- Article
First successful pregnancy following PGD for chromosome translocation on embryos generated from in-vitro matured oocytes: a case report.
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- Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2011, v. 22, n. 4, p. 371, doi. 10.1016/j.rbmo.2010.11.014
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- Article
Chromosome abnormality rates in human embryos obtained from in-vitro maturation and IVF treatment cycles.
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- Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2010, v. 21, n. 4, p. 552, doi. 10.1016/j.rbmo.2010.05.002
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- Publication type:
- Article
Expression of growth-differentiating factor 9 and its type 1 receptor in human ovaries.
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- Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2010, v. 21, n. 1, p. 109, doi. 10.1016/j.rbmo.2010.03.011
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- Article
Reliable preimplantation genetic diagnosis in thawed human embryos vitrified at cleavage stages without biopsy.
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- Journal of Assisted Reproduction & Genetics, 2011, v. 28, n. 7, p. 597, doi. 10.1007/s10815-011-9556-2
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- Publication type:
- Article
Different Probe Combinations for Assessment of Postzygotic Chromosomal Imbalances in Human Embryos.
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- Journal of Assisted Reproduction & Genetics, 2002, v. 19, n. 4, p. 177, doi. 10.1023/A:1014842012261
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- Publication type:
- Article
Direct Comparison of Detection Systems Used for the Development of Single-Cell Genetic Tests in....
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- Journal of Assisted Reproduction & Genetics, 2001, v. 18, n. 10, p. 557, doi. 10.1023/A:1011958008240
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- Article
Recurrent triploid digynic conceptions and mature ovarian teratomas: Are they different manifestations of the same genetic defect?
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- Genes, Chromosomes & Cancer, 2017, v. 56, n. 12, p. 832, doi. 10.1002/gcc.22484
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- Article
NLRP7 mutations in women with diploid androgenetic and triploid moles: a proposed mechanism for mole formation.
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- Human Molecular Genetics, 2009, v. 18, n. 24, p. 4907, doi. 10.1093/hmg/ddp461
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- Article
NLRP7 mutations in women with diploid androgenetic and triploid moles: a proposed mechanism for mole formation.
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- Human Molecular Genetics, 2009, v. 18, n. 5, p. 888, doi. 10.1093/hmg/ddn418
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- Publication type:
- Article