Works matching DE "PREIMPLANTATION genetic diagnosis"
Results: 1465
Genetic Counselling and Prenatal Diagnosis in a Case of Harlequin Ichthyosis: A Novel ABCA12 Gene Mutation.
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- Journal of Clinical & Diagnostic Research, 2025, v. 19, n. 2, p. 1, doi. 10.7860/JCDR/2025/74521.20614
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- Article
Navigating Hope and Complexity: Turkish Parents' Experiences with Savior Siblings.
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- Turkish Journal of Hematology, 2025, v. 42, n. 1, p. 47, doi. 10.4274/tjh.galenos.2025.2024.0419
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- Article
Screening Embryos for Genetic Diseases.
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- Innovation, 2004, v. 5, n. 1, p. 23
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- Article
Assisting Reproduction.
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- Innovation, 2004, v. 5, n. 1, p. 16
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- Article
Expression of adipokines in preimplantation rabbit and mice embryos.
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- Histochemistry & Cell Biology, 2008, v. 129, n. 6, p. 817, doi. 10.1007/s00418-008-0409-8
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- Article
Distribution of eosinophil granulocytes and mast cells in the reproductive tract of female goats in the preimplantation phase.
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- Veterinary Research Communications, 2009, v. 33, n. 6, p. 545, doi. 10.1007/s11259-009-9203-x
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- Article
Preimplantational Genetic Diagnosis and Mutation Detection in a Family with Duplication Mutation of DMD Gene.
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- Gynecologic & Obstetric Investigation, 2014, v. 78, n. 4, p. 272, doi. 10.1159/000365083
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- Article
Preimplantation Genetic Diagnosis:.
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- Gynecologic & Obstetric Investigation, 2005, v. 60, n. 1, p. 39, doi. 10.1159/000083483
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- Article
Accurate multiplex polymerase chain reaction assay for gender determination from a single cell.
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- 2000
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- journal article
PRENATAL GENDER SELECTION: MEDICAL, ETHICAL AND PSYCHOLOGICAL ASPECTS.
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- EUREKA: Health Sciences, 2023, n. 3, p. 58, doi. 10.21303/2504-5679.2023.003005
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- Article
PREIMPLANTATION GENETIC TESTING: A FUNDAMENTAL RIGHT.
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- William & Mary Journal of Race, Gender & Social Justice, 2022, v. 28, n. 3, p. 815
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- Article
Comprehensive chromosomal screening for preimplantation genetic testing: A mini-review.
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- Fertility Science & Research, 2023, v. 10, n. 4, p. 188, doi. 10.4103/fsr.fsr_41_23
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- Article
Male factor in recurrent pregnancy loss.
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- Fertility Science & Research, 2021, v. 8, n. 2, p. 105, doi. 10.4103/fsr.fsr_46_21
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- Article
PREIMPLANTATION GENETIC DIAGNOSIS: DEVELOPMENT AND REGULATION.
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- Medicine & Law (World Association for Medical Law), 2006, v. 25, n. 2, p. 365
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- Article
ETHICAL CONSIDERATIONS OF APPLICATIONS OF PREIMPLANTATION GENETIC DIAGNOSIS IN THE UNITED STATES.
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- Medicine & Law (World Association for Medical Law), 2003, v. 22, n. 3, p. 489
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- Article
How liberal is liberal eugenics?
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- Bioethica Forum, 2020, v. 13, n. 1, p. 31
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- Article
Preimplantation Genetic Testing Prevented Intergenerational Transmission of X-Linked Alport Syndrome.
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- Kidney Diseases, 2021, v. 7, n. 6, p. 514, doi. 10.1159/000517796
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- Article
PHYSIOLOGY AND ENDOCRINOLOGY SYMPOSIUM: Influence of cattle genotype (Bos indicus vs. Bos taurus) on oocyte and preimplantation embryo resistance to increased temperature.
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- Journal of Animal Science, 2013, v. 91, n. 3, p. 1143, doi. 10.2527/jas.2012-5802
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- Article
Involvement of free cholesterol and high-density lipoprotein in development and resistance of the preimplantation bovine embryo to heat shock.
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- Journal of Animal Science, 2012, v. 90, n. 11, p. 3762, doi. 10.2527/jas.2011-4717
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- Article
Mapping crossover events of mouse meiotic recombination by restriction fragment ligation-based Refresh-seq.
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- Cell Discovery, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41421-023-00638-9
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- Article
The Effect of Values and Secularism on Attitude towards Pre-Implantation Genetic Diagnosis of Embryos.
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- Social Sciences (2076-0760), 2018, v. 7, n. 11, p. 216, doi. 10.3390/socsci7110216
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- Article
Family With a Risk of Cancer Tries to Change Its Destiny.
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- Personalized Medicine in Oncology, 2014, v. 3, n. 2, p. 104
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- Article
DEVELOPMENTAL CAPACITY OF HUMAN EMBRYOS POSSESSING NUMERICAL CHROMOSOMAL ABNORMALITIES.
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- Bulletin of Taras Shevchenko National University of Kyiv / Vestnik Kievskogo Nacional'Nogo Universiteta Imeni Tarasa Ševčenko, 2013, v. 64, n. 2, p. 35
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- Article
Preimplantation genetic diagnosis in two families at risk for recurrence of Herlitz junctional epidermolysis bullosa.
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- Experimental Dermatology, 2000, v. 9, n. 4, p. 290, doi. 10.1034/j.1600-0625.2000.009004290.x
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- Article
Preimplantation genetic diagnosis of severe inherited skin diseases.
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- Experimental Dermatology, 1998, v. 7, n. 2/3, p. 65, doi. 10.1111/j.1600-0625.1998.tb00305.x
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- Article
Molecular autopsy for fetal structural anomaly: diagnostic and clinical utility of multidisciplinary team approach.
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- Ultrasound in Obstetrics & Gynecology, 2024, v. 64, n. 3, p. 381, doi. 10.1002/uog.27647
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- Article
Fetal ascites in third trimester as an unreported prenatal finding of Bardet-Biedl syndrome and successful subsequent unaffected livebirth assisted by preimplantation genetic diagnosis.
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- Ultrasound in Obstetrics & Gynecology, 2023, v. 61, n. 5, p. 649, doi. 10.1002/uog.26114
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- Article
VP33.07: Use of whole‐exome sequencing in establishing diagnosis of a rare metabolic disorder manifesting with multiple anomalies in a fetus.
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- Ultrasound in Obstetrics & Gynecology, 2020, v. 56, p. 195, doi. 10.1002/uog.22831
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- Article
EP11.19: Prenatal diagnosis and ultrasound features of harlequin ichthyosis.
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- Ultrasound in Obstetrics & Gynecology, 2018, v. 52, p. 248, doi. 10.1002/uog.19979
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- Article
Normal prenatal ultrasound findings reflect outcome in case of trisomy 14 confined placental mosaicism developing after preimplantation genetic diagnosis.
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- 2017
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- Case Study
Normal prenatal ultrasound findings reflect outcome in case of trisomy 14 confined placental mosaicism developing after preimplantation genetic diagnosis.
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- 2017
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- Publication type:
- Letter
EP10.29: Ultrasound characteristics in thoragopagus fetuses.
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- 2016
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- Publication type:
- journal article
Clinical management of woman with bleeding disorders: A survey among European haemophilia treatment centres.
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- Haemophilia, 2020, v. 26, n. 4, p. 657, doi. 10.1111/hae.14043
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- Article
Prenatal diagnosis and preimplantation genetic diagnosis: novel technologies and state of the art of PGD in different regions of the world.
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- Haemophilia, 2011, v. 17, p. 14, doi. 10.1111/j.1365-2516.2011.02559.x
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- Article
Preimplantation genetic diagnosis - a historical annotation: first PGD baby turns fifteen.
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- Haemophilia, 2011, v. 17, p. 18, doi. 10.1111/j.1365-2516.2011.02560.x
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- Article
Preimplantation genetic diagnosis: new reproductive options for carriers of haemophilia.
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- Haemophilia, 2004, v. 10, p. 126, doi. 10.1111/j.1365-2516.2004.01042.x
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- Article
Chromosome 17 translocation affects sperm morphology: Two case studies and literature review.
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- Andrologia, 2022, v. 54, n. 11, p. 1, doi. 10.1111/and.14620
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- Article
What Drives Embryo Development? Chromosomal Normality or Mitochondria?
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- Case Reports in Genetics, 2017, p. 1, doi. 10.1155/2017/4397434
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- Article
First Birth after Sperm Selection through Discontinuous Gradient Centrifugation and Artificial Insemination from a Chromosomal Translocation Carrier.
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- 2014
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- Publication type:
- Case Study
Genomic aspects in reproductive medicine.
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- Clinical & Experimental Reproductive Medicine, 2024, v. 51, n. 2, p. 91, doi. 10.5653/cerm.2023.06303
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- Article
Birth of a healthy baby after preimplantation genetic diagnosis in a carrier of mucopolysaccharidosis type II: The first case in Korea.
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- Clinical & Experimental Reproductive Medicine, 2019, v. 46, n. 4, p. 206
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- Article
A healthy delivery of twins by assisted reproduction followed by preimplantation genetic screening in a woman with X-linked dominant incontinentia pigmenti.
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- Clinical & Experimental Reproductive Medicine, 2014, v. 41, n. 4, p. 168, doi. 10.5653/cerm.2014.41.4.168
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- Article
Preimplantation genetic diagnosis for Charcot-Marie- Tooth disease.
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- Clinical & Experimental Reproductive Medicine, 2013, v. 40, n. 4, p. 163, doi. 10.5653/cerm.2013.40.4.163
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- Article
Successful birth with preimplantation genetic diagnosis using single-cell allele-specific PCR and sequencing in a woman with hypochondroplasia due to FGFR3 mutation (c.1620C>A, p.N540K).
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- Clinical & Experimental Reproductive Medicine, 2013, v. 40, n. 1, p. 42, doi. 10.5653/cerm.2013.40.1.42
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- Publication type:
- Article
Familial intragenic X-linked OPHN1 gene deletion in a newborn male infant with low birth weight and distinctive facial appearance that diagnosed by advanced microarray-CGH method.
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- Cumhuriyet Medical Journal, 2022, v. 44, n. 1, p. 125, doi. 10.7197/cmj.989474
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- Publication type:
- Article
A role of Pumilio 1 in mammalian oocyte maturation and maternal phase of embryogenesis.
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- Cell & Bioscience, 2018, v. 8, n. 1, p. N.PAG, doi. 10.1186/s13578-018-0251-1
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- Article
Identification of a novel homozygous mutation in the DDR2 gene from a patient with spondylo-meta-epiphyseal dysplasia by whole exome sequencing.
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- Iranian Journal of Basic Medical Sciences, 2021, v. 24, n. 2, p. 191, doi. 10.22038/IJBMS.2020.44487.10405
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- Article
Successful Pregnancy Following Preimplantation Genetic Diagnosis of Adrenoleukodystrophy by Detection of Mutation on the ABCD1 Gene.
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- Application of Clinical Genetics, 2021, v. 14, p. 313, doi. 10.2147/TACG.S318884
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- Publication type:
- Article
Preimplantation Genetic Diagnosis for DEB by Detecting a Novel Family-Specific COL7A1 Mutation in Vietnam.
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- Application of Clinical Genetics, 2021, v. 14, p. 467, doi. 10.2147/TACG.S344107
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- Publication type:
- Article
Procreative Beneficence and Genetic Enhancement.
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- Kriterion, 2018, v. 32, n. 1, p. 75, doi. 10.1515/krt-2018-320105
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- Publication type:
- Article