Found: 15
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Non-mosaic trisomy 20 presenting at 21 weeks' gestation as a thoraco-abdominal mass.
- Published in:
- Prenatal Diagnosis, 2001, v. 21, n. 5, p. 387, doi. 10.1002/pd.65
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- Article
Molecular cytogenetic analysis and clinical findings in a newborn with prenatally diagnosed rec(7)dup(7q)inv(7)(p22q31.3)pat.
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- Prenatal Diagnosis, 1999, v. 19, n. 12, p. 1150, doi. 10.1002/(SICI)1097-0223(199912)19:12<1150::AID-PD733>3.0.CO;2-0
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- Article
INCIDENCE AND SIGNIFICANCE OF CHROMOSOME MOSAICISM INVOLVING AN AUTOSOMAL STRUCTURAL ABNORMALITY DIAGNOSED PRENATALLY THROUGH AMNIOCENTESIS: A COLLABORATIVE STUDY.
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- Prenatal Diagnosis, 1996, v. 16, n. 1, p. 1, doi. 10.1002/(SICI)1097-0223(199601)16:1<1::AID-PD816>3.0.CO;2-W
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- Article
An accessory marker derived from chromosome 20 and its co-existence with a mosaic trisomy 20 cell line.
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- Prenatal Diagnosis, 1995, v. 15, n. 2, p. 123, doi. 10.1002/pd.1970150203
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- Article
Prenatal identification of small mosaic markers of different chromosomal origins.
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- Prenatal Diagnosis, 1992, v. 12, n. 2, p. 83, doi. 10.1002/pd.1970120203
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- Article
In utero Hematopoietic Stem Cell Transplantation in Canines: Exploring the Gestational Age Window of Opportunity to Maximize Engraftment.
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- Fetal Diagnosis & Therapy, 2013, v. 33, n. 2, p. 116, doi. 10.1159/000346211
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- Article
X inactivation in triploidy and trisomy: the search for autosomal transfactors that choose the active X.
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- European Journal of Human Genetics, 2008, v. 16, n. 2, p. 153, doi. 10.1038/sj.ejhg.5201944
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- Article
Ring Chromosome 21: Characterization of DNA Sequences at Sites of Breakage and Reunion.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 33, doi. 10.1111/j.1749-6632.1985.tb21481.x
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- Article
Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome.
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- Mammalian Genome, 2000, v. 11, n. 11, p. 1000, doi. 10.1007/s003350010193
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- Article
Clinical consequences of an increasing trend of preferential use of cultured villi for molecular diagnosis by CVS.
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- Prenatal Diagnosis, 2008, v. 28, n. 4, p. 332, doi. 10.1002/pd.1953
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- Article
Microphthalmia with linear skin defects (MLS) syndrome evaluated by prenatal karyotyping, FISH and array comparative genomic hybridization.
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- Prenatal Diagnosis, 2007, v. 27, n. 4, p. 373, doi. 10.1002/pd.1674
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- Article
Prenatal Detection of a Subtle Unbalanced Chromosome Rearrangement by Karyotyping, FISH and Array Comparative Genomic Hybridization.
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- Fetal Diagnosis & Therapy, 2008, v. 24, n. 3, p. 286, doi. 10.1159/000158519
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- Article
Use of T-Cell Antibodies for Donor Dosaging in a Canine Model of in utero Hematopoietic Stem Cell Transplantation.
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- Fetal Diagnosis & Therapy, 2007, v. 22, n. 3, p. 175, doi. 10.1159/000098711
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- Article
Prenatal Detection of an Interstitial Deletion in 4p15 in a Fetus with an Increased Nuchal Skin Fold Measurement.
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- Fetal Diagnosis & Therapy, 2005, v. 20, n. 1, p. 58, doi. 10.1159/000081371
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- Article
Cloning and characterization of a secreted frizzled-related protein that is expressed by the retinal pigment epithelium.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 4, p. 575, doi. 10.1093/hmg/8.4.575
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- Article