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You searched for: Author/Creator Scott, Daryl A.

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1. A Comprehensive Assessment of Co-occurring Birth Defects among Infants with Non-Syndromic Anophthalmia or Microphthalmia. (3rd September 2021)

2. A novel, de novo intronic variant in POGZ causes White–Sutton syndrome. Issue 7 (9th April 2022)

4. Atypical Alexander disease with dystonia, retinopathy, and a brain mass mimicking astrocytoma. (August 2018)

5. BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorder. Issue 5 (7th February 2020)

6. Birth Defect Co-Occurrence Patterns Among Infants With Cleft Lip and/or Palate. (April 2022)

7. Birth defects that co‐occur with non‐syndromic gastroschisis and omphalocele. Issue 11 (4th September 2020)

9. Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1. Issue 1 (26th October 2019)

10. Congenital diaphragmatic hernia as a prominent feature of a SPECC1L‐related syndrome. Issue 12 (21st September 2020)