Search

Search Constraints

You searched for: Author/Creator Schwartz Ida guestEditor.

Search Results

1. Adaptation and co‐adaptation of skin pigmentation and vitamin D genes in native Americans. Issue 4 (15th December 2020)

2. An international telemedicine program for diagnosis of genetic disorders: Partnership of pediatrician and geneticist. Issue 4 (21st November 2020)

3. Autosomal dominant early onset Alzheimer's disease in the Mexican state of Jalisco: High frequency of the mutation PSEN1 c.1292C>A and phenotypic profile of patients. Issue 4 (4th December 2020)

4. Biased pathogenic assertions of loss of function variants challenge molecular diagnosis of admixed individuals. Issue 3 (29th June 2021)

5. Brazil's Craniofacial Project: Different approaches on orofacial clefts and 22q11.2 deletion syndrome. Issue 4 (9th November 2020)

6. Case report: Maternal tyrosinemia type 1a under NTBC treatment with tyrosine‐ and phenylalanine restricted diet in Chile. Issue 4 (10th December 2020)

7. Clinical and molecular analysis of 26 individuals with Noonan syndrome in a reference institution in Colombia. Issue 4 (10th December 2020)

8. Clinical trials for genetic diseases in Latin America. Issue 3 (3rd September 2021)