Found: 9
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Utilization of genetic testing: Analysis of 4,499 prior authorization requests for molecular genetic tests at four US regional health plans.
- Published in:
- Journal of Genetic Counseling, 2022, v. 31, n. 3, p. 771, doi. 10.1002/jgc4.1543
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- Article
Cover Image, Volume 176A, Number 4, April 2018.
- Published in:
- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 4, p. 1, doi. 10.1002/ajmg.a.38671
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- Publication type:
- Article
Natural history and genotype‐phenotype correlations in 72 individuals with <italic>SATB2</italic>‐associated syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 4, p. 925, doi. 10.1002/ajmg.a.38630
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- Article
The role of IQSEC2 in syndromic intellectual disability: Narrowing the diagnostic odyssey.
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- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 10, p. 2814, doi. 10.1002/ajmg.a.38404
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- Article
SMARCE1, a rare cause of Coffin-Siris Syndrome: Clinical description of three additional cases.
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- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 8, p. 1967, doi. 10.1002/ajmg.a.37722
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- Article
First clinical report of an infant with microcephaly and CASC5 mutations.
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 8, p. 2215, doi. 10.1002/ajmg.a.37726
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- Article
COL1A1 and COL1A2 sequencing results in cohort of patients undergoing evaluation for potential child abuse.
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- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 7, p. 1858, doi. 10.1002/ajmg.a.37664
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- Article
Cardiovascular and genitourinary anomalies in patients with duplications within the Williams syndrome critical region: Phenotypic expansion and review of the literature.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 8, p. 1998, doi. 10.1002/ajmg.a.36601
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- Article
Molecular and Cytogenetic Evaluation of a Patient with Ring Chromosome 13 and Discordant Results.
- Published in:
- Cytogenetic & Genome Research, 2014, v. 144, n. 2, p. 104, doi. 10.1159/000368649
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- Article