Found: 13
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Treatment of Two Infants with Cooley's Anemia with Sodium Phenylbutyrate.
- Published in:
- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 452, doi. 10.1111/j.1749-6632.1998.tb10518.x
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- Article
Hemoglobin E/β Thalassemia: The Canadian Experience.
- Published in:
- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 410, doi. 10.1111/j.1749-6632.1998.tb10506.x
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- Publication type:
- Article
Determination of a kinship system using ancient DNA, mortuary practice, and historic records in an upper Canadian pioneer cemetery.
- Published in:
- International Journal of Osteoarchaeology, 2003, v. 13, n. 4, p. 232, doi. 10.1002/oa.680
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- Publication type:
- Article
Molecular phenotype and bleeding risks of an inherited platelet disorder in a family with a RUNX1 frameshift mutation.
- Published in:
- Haemophilia, 2017, v. 23, p. e204, doi. 10.1111/hae.13169
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- Publication type:
- Article
Genetic linkage studies in antithrombin-deficient kindreds using a highly polymorphic trinucleotide short tandem repeat (str) within the human antithrombin gene.
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- American Journal of Hematology, 1994, v. 46, n. 2, p. 107, doi. 10.1002/ajh.2830460210
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- Publication type:
- Article
Compound Heterozygosity For Triplicated α-Globin Gene and (– –<sup>SEA</sup>) α-Globin Gene Deletion: Implication For Thalassaemia Screening.
- Published in:
- British Journal of Haematology, 2000, v. 110, n. 2, p. 493, doi. 10.1046/j.1365-2141.2000.02165-1.x
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- Publication type:
- Article
Parentage testing implications of male fertility after allogeneic bone marrow transplantation.
- Published in:
- Bone Marrow Transplantation, 1999, v. 23, n. 2, p. 187, doi. 10.1038/sj.bmt.1701519
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- Publication type:
- Article
Krüppel-like factor 1: hematologic phenotypes associated with KLF1 gene mutations.
- Published in:
- International Journal of Laboratory Hematology, 2015, v. 37, p. 78, doi. 10.1111/ijlh.12356
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- Publication type:
- Article
Krüppel-like factor 1: hematologic phenotypes associated with KLF1 gene mutations.
- Published in:
- 2015
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- Publication type:
- Journal Article
Diagnostic testing for α-globin gene disorders in a heterogeneous North American population.
- Published in:
- 2013
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- Publication type:
- Journal Article
Diagnostic testing for α-globin gene disorders in a heterogeneous North American population.
- Published in:
- International Journal of Laboratory Hematology, 2013, v. 35, n. 3, p. 306, doi. 10.1111/ijlh.12066
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- Publication type:
- Article
DHCR7mutations and genotype–phenotype correlation in 37 Polish patients with Smith–Lemli–Opitz syndrome.
- Published in:
- Clinical Genetics, 2004, v. 66, n. 6, p. 517, doi. 10.1111/j.1399-0004.2004.00350.x
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- Publication type:
- Article
A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 216, doi. 10.1111/j.1399-0004.1990.tb03505.x
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- Publication type:
- Article