Found: 15
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Syndromic craniosynostosis, fibroblast growth factor receptor 2 ( FGFR2) mutations, and sacrococcygeal eversion presenting as human tails.
- Published in:
- Child's Nervous System, 2012, v. 28, n. 8, p. 1221, doi. 10.1007/s00381-012-1813-x
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- Publication type:
- Article
Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 5, p. 547, doi. 10.1038/ejhg.2010.237
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- Publication type:
- Article
Sensitivity of human placental monooxygenase activity to maternal smoking.
- Published in:
- Clinical Pharmacology & Therapeutics, 1981, v. 30, n. 5, p. 687, doi. 10.1038/clpt.1981.221
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- Publication type:
- Article
Recessive mutations in EPG5 cause Vici syndrome, a multisystem disorder with defective autophagy.
- Published in:
- Nature Genetics, 2013, v. 45, n. 1, p. 83, doi. 10.1038/ng.2497
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- Publication type:
- Article
Assessment of multiple types of DNA damage in human placentas from smoking and nonsmoking women in the Czech Republic.
- Published in:
- Environmental & Molecular Mutagenesis, 2011, v. 52, n. 1, p. 58, doi. 10.1002/em.20581
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- Publication type:
- Article
Accuracy of ultrasound diagnoses in pregnancies complicated by suspected fetal anomalies.
- Published in:
- Prenatal Diagnosis, 1988, v. 8, n. 2, p. 109, doi. 10.1002/pd.1970080205
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- Publication type:
- Article
Case report of myometrial window following fetoscopic treatment of twin-twin transfusion syndrome: indications of underlying collagen vascular disease?
- Published in:
- Clinical Case Reports, 2017, v. 5, n. 6, p. 975, doi. 10.1002/ccr3.885
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- Publication type:
- Article
Sensitivity of somatic mutations in human umbilical cord blood to maternal environments.
- Published in:
- Environmental & Molecular Mutagenesis, 1995, v. 26, n. 3, p. 203, doi. 10.1002/em.2850260304
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- Publication type:
- Article
Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features.
- Published in:
- 2017
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- Publication type:
- Erratum
Fetal Heart Rate in Relation to Body Mass.
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- Proceedings of the Society for Experimental Biology & Medicine, 1983, v. 172, n. 1, p. 107, doi. 10.3181/00379727-172-41535
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- Publication type:
- Article
Recent Developments in Molecular Epidemiology: A Study of the Effects of Environmental Polycyclic Aromatic Hydrocarbons on Birth Outcomes in Poland.
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- American Journal of Epidemiology, 1998, v. 147, n. 3, p. 309, doi. 10.1093/oxfordjournals.aje.a009451
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- Publication type:
- Article
Innovation Drives Change - Impacts the Air Force and Airmen.
- Published in:
- Armed Forces Comptroller, 2019, v. 64, n. 1, p. 47
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- Publication type:
- Article
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggests a single entity with Cowden syndrome.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 8, p. 1461, doi. 10.1093/hmg/8.8.1461
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- Publication type:
- Article
Human doublecortin (DCX ) and the homologous gene in mouse encode a putative Ca[sup 2+]-dependent signaling protein which is mutated in human X-linked neuronal migration defects.
- Published in:
- Human Molecular Genetics, 1998, v. 7, n. 8, p. 1327
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- Publication type:
- Article
Abstracts.
- Published in:
- 1999
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- Publication type:
- Abstract