Found: 13
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The Prognostic Effect of CDKN2A/2B Gene Deletions in Pediatric Acute Lymphoblastic Leukemia (ALL): Independent Prognostic Significance in BFM-Based Protocols.
- Published in:
- Diagnostics (2075-4418), 2023, v. 13, n. 9, p. 1589, doi. 10.3390/diagnostics13091589
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- Article
Familial Aggregation of a Novel Missense Variant of COL2A1 Gene Associated with Short Extremities: Case Report and Review of the Literature.
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- Children, 2022, v. 9, n. 8, p. 1229, doi. 10.3390/children9081229
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- Article
Copy Number Alteration Profile Provides Additional Prognostic Value for Acute Lymphoblastic Leukemia Patients Treated on BFM Protocols.
- Published in:
- Cancers, 2021, v. 13, n. 13, p. 3289, doi. 10.3390/cancers13133289
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- Article
Low-Level Trisomy 14 Mosaicism: A Carrier of an Isochromosome 14 and a Supernumerary Marker Chromosome 14.
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- Cytogenetic & Genome Research, 2020, v. 160, n. 11/12, p. 664, doi. 10.1159/000511549
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- Article
FGFR3 related skeletal dysplasias diagnosed prenatally by ultrasonography and molecular analysis: Presentation of 17 cases.
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- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 10, p. 2426, doi. 10.1002/ajmg.a.34189
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- Article
Erratum: Prenatal diagnosis of a de novo partial trisomy 10p12.1-12.2 pter originating from an unbalanced translocation onto 15qter and confirmed with array CGH.
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- Prenatal Diagnosis, 2010, v. 30, n. 6, p. 594, doi. 10.1002/pd.2558
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- Article
Endothelial nitric oxide synthase gene polymorphisms in recurrent spontaneous abortions.
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- Archives of Gynecology & Obstetrics, 2008, v. 278, n. 4, p. 349, doi. 10.1007/s00404-008-0577-8
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- Article
Prenatal diagnosis of a de novo partial trisomy 10p12.1-12.2 pter originating from an unbalanced translocation onto 15qter and confirmed with array CGH.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 8, p. 770, doi. 10.1002/pd.2049
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- Article
Prenatal diagnosis of common aneuploidies using quantitative fluorescent PCR.
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- Prenatal Diagnosis, 2002, v. 22, n. 5, p. 360, doi. 10.1002/pd.301
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- Article
BRCA1 mutation analysis in breast/ovarian cancer families from Greece.
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- Human Mutation, 2000, v. 16, n. 3, p. 272, doi. 10.1002/1098-1004(200009)16:3<272::AID-HUMU17>3.0.CO;2-4
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- Article
Screening for minor changes in the distal part of the human dystrophin gene in Greek DMD/BMD patients.
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- European Journal of Human Genetics, 1999, v. 7, n. 2, p. 179, doi. 10.1038/sj.ejhg.5200253
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- Article
Molecular Analysis and Electromyoneurographic Abnormalities in Croatian Children with Proximal Spinal Muscular Atrophies.
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- Clinical Chemistry & Laboratory Medicine, 1998, v. 36, n. 8, p. 667
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- Article
3′ acceptor splice site mutation in intron 50 leads to mild duchenne muscular dystrophy phenotype.
- Published in:
- Human Mutation, 1998, v. 11, p. S209, doi. 10.1002/humu.1380110168
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- Article