Autism spectrum disorder and achondroplasia in an Egyptian patient.
- Published in:
- Middle East Journal of Medical Genetics, 2021, v. 10, n. 2, p. 101, doi. 10.4103/mxe.mxe_7_21
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- Publication type:
- Article
Works matching IS 20908571 AND DT 2021 AND VI 10 AND IP 2
Results: 7
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Frequent genetic disorders associated with missing teeth and revisiting classification of anodontia: a retrospective study.
- Published in:
- Middle East Journal of Medical Genetics, 2021, v. 10, n. 2, p. 95, doi. 10.4103/mxe.mxe_1_22
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- Publication type:
- Article
3
Biochemical evaluations at two time points in 15 patients with nephropathic cystinosis under cysteamine treatment.
- Published in:
- Middle East Journal of Medical Genetics, 2021, v. 10, n. 2, p. 89, doi. 10.4103/mxe.mxe_12_21
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- Publication type:
- Article
4
Cytokine profile in a cohort of Egyptian patients with autism spectrum disorders.
- Published in:
- Middle East Journal of Medical Genetics, 2021, v. 10, n. 2, p. 83, doi. 10.4103/mxe.mxe_10_21
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- Publication type:
- Article
5
Case of autosomal-recessive spinal muscular atrophy with respiratory distress type 1 caused by compound heterozygous mutations in immunoglobulin-binding protein 2 gene: expansion in clinical features.
- Published in:
- Middle East Journal of Medical Genetics, 2021, v. 10, n. 2, p. 76, doi. 10.4103/mxe.mxe_8_21
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- Publication type:
- Article
6
Molecular and cytogenetic diagnosis of disorders/differences of sex development: molecular update of genes controlling sexual differentiation.
- Published in:
- Middle East Journal of Medical Genetics, 2021, v. 10, n. 2, p. 58, doi. 10.4103/mxe.mxe_14_21
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- Publication type:
- Article
7
Professor Samia Temtamy: the founder of human genetics at the National Research Centre, Egypt.
- Published in:
- Middle East Journal of Medical Genetics, 2021, v. 10, n. 2, p. 51, doi. 10.4103/mxe.mxe_13_21
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- Publication type:
- Article