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Strengthening the Evidence: Similar Rates of Neural Tube Defects Among Deliveries Regardless of Maternal HIV Status and Dolutegravir Exposure in Hospital Birth Surveillance in Eswatini.
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- Open Forum Infectious Diseases, 2023, v. 10, n. 9, p. 1, doi. 10.1093/ofid/ofad441
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- Publication type:
- Article
Birth defects and military service since 1990.
- Published in:
- 2009
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- Publication type:
- journal article
Birth Defects and Military Service Since 1990.
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- Military Medicine, 2009, v. 174, n. 2, p. 170
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- Publication type:
- Article
Asymmetric faces: Symbolic, spiritual, and representative.
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- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2021, v. 187, n. 2, p. 278, doi. 10.1002/ajmg.c.31901
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- Publication type:
- Article
Response to Mariani Et al.: A Second Report of PARK2 Duplication and Developmental Delay.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 5, p. 484, doi. 10.1002/ajmg.b.32172
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- Publication type:
- Article
The multiple de novo copy number variant (MdnCNV) phenomenon presents with peri-zygotic DNA mutational signatures and multilocus pathogenic variation.
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- Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01123-w
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- Publication type:
- Article
Classification of isolated versus multiple birth defects: An automated process for population‐based registries.
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- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 10, p. 1, doi. 10.1002/ajmg.a.63714
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- Publication type:
- Article
Prevalence and descriptive epidemiology of choanal atresia and stenosis in Texas, 1999–2018.
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- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 6, p. 1, doi. 10.1002/ajmg.a.63549
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- Publication type:
- Article
Biallelic variants in NUDCD2 associated with a multiple malformation syndrome with cholestasis and renal failure.
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- American Journal of Medical Genetics. Part A, 2023, v. 191, n. 9, p. 2324, doi. 10.1002/ajmg.a.63314
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- Publication type:
- Article
Patterns of co‐occurring birth defects in children with anotia and microtia.
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- American Journal of Medical Genetics. Part A, 2023, v. 191, n. 3, p. 805, doi. 10.1002/ajmg.a.63081
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- Publication type:
- Article
Identifying syndromes in studies of structural birth defects: Guidance on classification and evaluation of potential impact.
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- American Journal of Medical Genetics. Part A, 2023, v. 191, n. 1, p. 190, doi. 10.1002/ajmg.a.63014
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- Publication type:
- Article
Patterns of congenital anomalies among individuals with trisomy 13 in Texas.
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- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 6, p. 1787, doi. 10.1002/ajmg.a.62175
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- Publication type:
- Article
Birth defects that co‐occur with non‐syndromic gastroschisis and omphalocele.
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- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 11, p. 2581, doi. 10.1002/ajmg.a.61830
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- Publication type:
- Article
An additional case of Néstor‐Guillermo progeria syndrome diagnosed in early childhood.
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- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 10, p. 2399, doi. 10.1002/ajmg.a.61777
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- Publication type:
- Article
Likelihood of meeting defined VATER/VACTERL phenotype in infants with esophageal atresia with or without tracheoesophageal fistula.
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- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 11, p. 2202, doi. 10.1002/ajmg.a.61337
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- Publication type:
- Article
Incontinentia pigmenti in adults.
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- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 8, p. 1415, doi. 10.1002/ajmg.a.61205
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- Publication type:
- Article
An additional case of Hennekam lymphangiectasia–lymphedema syndrome caused by loss‐of‐function mutation in ADAMTS3.
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- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 12, p. 2858, doi. 10.1002/ajmg.a.40633
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- Publication type:
- Article
A modified panel of sentinel congenital anomalies for potential use in mutation epidemiology based on birth defects registry data.
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 9, p. 2187, doi. 10.1002/ajmg.a.36623
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- Publication type:
- Article
The childless man.
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 2, p. 561, doi. 10.1002/ajmg.a.36290
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- Publication type:
- Article
Birth Defect Co-Occurrence Patterns Among Infants With Cleft Lip and/or Palate.
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- Cleft Palate Craniofacial Journal, 2022, v. 59, n. 4, p. 417, doi. 10.1177/10556656211010060
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- Publication type:
- Article
Pre-Zika descriptive epidemiology of microcephaly in Texas, 2008-2012.
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- Birth Defects Research, 2018, v. 110, n. 5, p. 395, doi. 10.1002/bdr2.1164
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- Publication type:
- Article
Prune belly syndrome in surviving males can be caused by Hemizygous missense mutations in the X-linked Filamin A gene.
- Published in:
- BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-0973-x
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- Publication type:
- Article
The Antiretroviral Pregnancy Registry: Three decades of prospective monitoring for birth defects.
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- Pharmacoepidemiology & Drug Safety, 2024, v. 33, n. 6, p. 1, doi. 10.1002/pds.5801
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- Publication type:
- Article
Clinical Exome Studies Have Inconsistent Coverage.
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- Clinical Chemistry, 2020, v. 66, n. 1, p. 199, doi. 10.1093/clinchem.2019.306795
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- Publication type:
- Article
Sunspot activity and birth defects among Texas births (1999–2016).
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- Birth Defects Research, 2023, v. 115, n. 12, p. 1120, doi. 10.1002/bdr2.2206
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- Publication type:
- Article
Risk factors and time trends for isolated craniosynostosis.
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- Birth Defects Research, 2021, v. 113, n. 1, p. 43, doi. 10.1002/bdr2.1824
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- Publication type:
- Article
Acculturation and selected birth defects among non‐Hispanic Blacks in a population‐based case–control study.
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- Birth Defects Research, 2020, v. 112, n. 7, p. 535, doi. 10.1002/bdr2.1665
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- Publication type:
- Article
Defect evaluation by infant photographs in a multicenter pharmaceutical clinical trial.
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- Birth Defects Research, 2020, v. 112, n. 1, p. 118, doi. 10.1002/bdr2.1619
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- Publication type:
- Article
Co‐occurring defect analysis: A platform for analyzing birth defect co‐occurrence in registries.
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- Birth Defects Research, 2019, v. 111, n. 18, p. 1356, doi. 10.1002/bdr2.1549
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- Publication type:
- Article
Levetiracetam Pregnancy Registry: Final results and a review of the impact of registry methodology and definitions on the prevalence of major congenital malformations.
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- Birth Defects Research, 2019, v. 111, n. 13, p. 872, doi. 10.1002/bdr2.1526
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- Publication type:
- Article
Selected acculturation factors and birth defects in the National Birth Defects Prevention Study, 1997–2011.
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- Birth Defects Research, 2019, v. 111, n. 10, p. 598, doi. 10.1002/bdr2.1494
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- Publication type:
- Article
Temporal trends in diagnoses of congenital microcephaly, Texas Hospital Discharge Diagnoses, 2000–2015.
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- Birth Defects Research, 2019, v. 111, n. 10, p. 584, doi. 10.1002/bdr2.1491
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- Publication type:
- Article
Neonatal presentation of ventricular tachycardia and a Reye-like syndrome episode associated with disturbed mitochondrial energy metabolism.
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- BMC Pediatrics, 2002, v. 2, p. 12, doi. 10.1186/1471-2431-2-12
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- Publication type:
- Article
Enamel Pit Defects and Taurodontism in a Patient with Ring Chromosome 14 and 47,XXX.
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- Journal of Dentistry for Children, 2017, v. 84, n. 1, p. 39
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- Publication type:
- Article
Pregnancy Outcomes After Exposure to Certolizumab Pegol.
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- Arthritis & Rheumatology, 2018, v. 70, n. 9, p. 1399, doi. 10.1002/art.40508
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- Publication type:
- Article
NEURAL TUBE AND OTHER BIRTH DEFECTS BY HIV STATUS AND ART REGIMEN IN ESWATINI.
- Published in:
- Topics in Antiviral Medicine, 2023, v. 31, n. 2, p. 316
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- Publication type:
- Article
Overcoming presynaptic effects of VAMP2 mutations with 4‐aminopyridine treatment.
- Published in:
- Human Mutation, 2020, v. 41, n. 11, p. 1999, doi. 10.1002/humu.24109
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- Publication type:
- Article
Expanding the Molecular and Clinical Phenotype of SSR4-CDG.
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- Human Mutation, 2015, v. 36, n. 11, p. 1048, doi. 10.1002/humu.22856
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- Publication type:
- Article
Insight into IKBKG/ NEMO Locus: Report of New Mutations and Complex Genomic Rearrangements Leading to Incontinentia Pigmenti Disease.
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- Human Mutation, 2014, v. 35, n. 2, p. 165, doi. 10.1002/humu.22483
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- Publication type:
- Article
Pharmacovigilance pregnancy data in a large population of patients with chronic inflammatory disease exposed to certolizumab pegol.
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- Therapeutic Advances in Musculoskeletal Disease, 2022, p. 1, doi. 10.1177/1759720X221087650
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- Publication type:
- Article
Selection Against Mutant Alleles in Blood Leukocytes is a Consistent Feature in Incontinentia Pigmenti Type 2.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 11, p. 1777, doi. 10.1093/hmg/5.11.1777
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- Publication type:
- Article