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You searched for: Author/Creator Brooks, Alice S.

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1. An overview of health issues and development in a large clinical cohort of children with Angelman syndrome. Issue 1 (15th November 2019)

2. Goldberg–Shprintzen syndrome is determined by the absence, or reduced expression levels, of KIFBP. Issue 11 (16th September 2020)

4. Infantile hypertrophic pyloric stenosis in patients with esophageal atresia. Issue 9 (16th April 2020)

6. Multidisciplinary interaction and MCD gene discovery. The perspective of the clinical geneticist. (November 2021)

7. No major role for periconceptional folic acid use and its interaction with the MTHFR C677T polymorphism in the etiology of congenital anorectal malformations. Issue 6 (20th May 2014)

8. Novel FOXF1 Mutations in Sporadic and Familial Cases of Alveolar Capillary Dysplasia with Misaligned Pulmonary Veins Imply a Role for its DNA Binding Domain. Issue 6 (12th April 2013)

9. Novel no‐stop FLNA mutation causes multi‐organ involvement in males. Issue 9 (19th July 2013)

10. Novel no‐stop FLNA mutation causes multi‐organ involvement in males. Issue 9 (19th July 2013)