Found: 6
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Janiceps Conjoined Twins with Extreme Asymmetry: Case Report with Complete Autopsy and Histopathologic Findings.
- Published in:
- Pediatric & Developmental Pathology, 2009, v. 12, n. 5, p. 374, doi. 10.2350/08-11-0555.1
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- Article
Interstitial deletion 2(p11.2p13): a rare chromosomal abnormality.
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- Clinical Genetics, 1997, v. 52, n. 1, p. 61, doi. 10.1111/j.1399-0004.1997.tb02516.x
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- Article
Intestinal Ganglioneuromatosis: Unusual Presentation of Cowden Syndrome Resulting in Delayed Diagnosis.
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 5, p. 1085, doi. 10.1002/ajmg.a.35731
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- Article
Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes.
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- European Journal of Human Genetics, 2012, v. 20, n. 7, p. 754, doi. 10.1038/ejhg.2012.6
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- Article
Pathogenic Mutations in Cancer-Predisposing Genes: A Survey of 300 Patients with Whole-Genome Sequencing and Lifetime Electronic Health Records.
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- PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0167847
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- Article
Variable outcomes in mosaic trisomy 16: five case reports and literature analysis.
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- Prenatal Diagnosis, 2006, v. 26, n. 5, p. 454, doi. 10.1002/pd.1437
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- Article