Found: 13
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Effect of cryopreservation on the frequency of chromosomal abnormalities and sex ratio in human sperm.
- Published in:
- Molecular Reproduction & Development, 1991, v. 30, n. 2, p. 159, doi. 10.1002/mrd.1080300213
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- Publication type:
- Article
Review of the recurrent 8q13.2q13.3 branchio-oto-renal related microdeletion, and report of an additional case with associated distal arthrogryposis.
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 11, p. 2984, doi. 10.1002/ajmg.a.37695
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- Publication type:
- Article
A 2q24.3q31.1 microdeletion found in a patient with Filippi-like syndrome phenotype: A case report.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 9, p. 2385, doi. 10.1002/ajmg.a.36636
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- Publication type:
- Article
Duplication of the 22q11.2 region associated with congenital cardiac disease.
- Published in:
- Cardiology in the Young, 2005, v. 15, n. 2, p. 229, doi. 10.1017/S1047951105000466
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- Publication type:
- Article
Unusual segregation products in sperm from a pericentric inversion 17 heterozygote.
- Published in:
- Human Genetics, 2005, v. 117, n. 4, p. 357, doi. 10.1007/s00439-004-1245-0
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- Publication type:
- Article
Aneuploid spermatozoa in infertile men: Teratozoospermia.
- Published in:
- Molecular Reproduction & Development, 2002, v. 61, n. 2, p. 200, doi. 10.1002/mrd.1148
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- Publication type:
- Article
Failure of NIPT to detect constitutional chromoanasynthesis involving chromosome 21 in a case of fetal hydrops—A case report.
- Published in:
- Clinical Case Reports, 2019, v. 7, n. 11, p. 2165, doi. 10.1002/ccr3.2369
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- Publication type:
- Article
Chromosome analysis of spermatozoa extracted from testes of men with non-obstructive azoospermia.
- Published in:
- 2000
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- Publication type:
- journal article
Application of Microarray-Based Comparative Genomic Hybridization in Prenatal and Postnatal Settings: Three Case Reports.
- Published in:
- Genetics Research International, 2011, p. 1, doi. 10.4061/2011/976398
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- Publication type:
- Article
Mosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns-like phenotype.
- Published in:
- 2017
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- Publication type:
- journal article
Interstitial deletion of 11q in a mother and fetus: implications of directly transmitted chromosomal imbalances for prenatal genetic counseling.
- Published in:
- Prenatal Diagnosis, 2009, v. 29, n. 3, p. 283, doi. 10.1002/pd.2209
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- Publication type:
- Article
Shedding new light on false positive diagnosis of trisomy 21 by fluorescence in situ hybridization (FISH) on uncultured amniotic fluid cells: experiences from two Canadian cytogenetic laboratories.
- Published in:
- Prenatal Diagnosis, 2007, v. 27, n. 10, p. 964, doi. 10.1002/pd.1795
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- Publication type:
- Article
Cri du chat syndrome due to meiotic recombination in a pericentric inversion 5 carrier.
- Published in:
- Clinical Genetics, 1992, v. 41, n. 5, p. 266, doi. 10.1111/j.1399-0004.1992.tb03679.x
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- Publication type:
- Article