Hb Madrid or alpha 2 beta (2)115(G17)Ala-->Pro in a black teenager

Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura.

Nature·2001

Uterine perforation from induced abortion at Korle Bu Teaching Hospital, Accra, Ghana: a five year review.

West African journal of medicine·2000

A descriptive study of the frequency and characteristics of proliferative enteropathy in swine in Ontario by analyzing routine animal health surveillance data.

The Canadian veterinary journal = La revue veterinaire canadienne·1999

Antenatal haemoglobin profile at Korle-Bu Teaching Hospital.

East African medical journal·1999

A simulation model for studying the role of pre-slaughter factors on the exposure of beef carcasses to human microbial hazards.

Preventive veterinary medicine·1999

Pre-slaughter control of Escherichia coli O157 in beef cattle: a simulation study.

Preventive veterinary medicine·1999

Genotype-Specific Hematologic Signatures Across α-Globin Defect Categories in α-Thalassemia.

Hemoglobin·2026

Mapping the Management-to-Cure Transition in Thalassemia Research: Semantic Topic Modeling of 17,651 Publications Across Three Decades.

Hemoglobin·2026

Uncovering the True Genotype: Unusually Severe Sickle Cell Disease in a Child with an Initial HbSC Diagnosis.

Hemoglobin·2026

Ocular Complications Among Patients with Beta-Thalassaemia Major and Intermedia: A Comparative Study from Pakistan.

Hemoglobin·2026

Psychometric Performance of the Adult Sickle Cell Quality-of-Life Measurement Information System (ASCQ-Me) in Jamaicans with Sickle Cell Disease.

Hemoglobin·2026

Co-Heredity of (-α)20.5 Deletion and IVS I-1 G > A (HBB: C.92 + 1 G > A) Mutations in a Pediatric Patient: A Cause of Moderate Anemia Phenotype?

Hemoglobin·2026

A 21-Year Diagnostic Odyssey in TBC1D24-Associated Developmental and Epileptic Encephalopathy With Favorable Response to Corpus Callosotomy: A Case Report.

Cureus·2026

Male Goltz Syndrome due to Postzygotic PORCN Mosaicism: A Case Report.

Case reports in dermatological medicine·2026

Characterization of ntrk receptors and bdnf ligand in Cynoglossus semilaevis provides molecular insights into sexual size dimorphism regulation in flatfish.

Comparative biochemistry and physiology. Part A, Molecular & integrative physiology·2026

Late diagnosis of Gitelman syndrome in an elderly patient: identification of a novel SLC12A3 pathogenic variant.

Jornal brasileiro de nefrologia·2026

Sex-ratio distorters enable pre-zygotic sexing for sex-specific transcriptomics in Anopheles gambiae embryos.

Cell reports·2026

Asymmetric Functional Divergence of alx4a and alx4b in Iridophore Differentiation and Cranial Development in Nile Tilapia.

Cells·2026

Related Experiment Videos

Hb Madrid or alpha 2 beta (2)115(G17)Ala-->Pro in a black teenager

Related Concept Videos

Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura.

Uterine perforation from induced abortion at Korle Bu Teaching Hospital, Accra, Ghana: a five year review.

A descriptive study of the frequency and characteristics of proliferative enteropathy in swine in Ontario by analyzing routine animal health surveillance data.

Antenatal haemoglobin profile at Korle-Bu Teaching Hospital.

A simulation model for studying the role of pre-slaughter factors on the exposure of beef carcasses to human microbial hazards.

Pre-slaughter control of Escherichia coli O157 in beef cattle: a simulation study.

Genotype-Specific Hematologic Signatures Across α-Globin Defect Categories in α-Thalassemia.

Mapping the Management-to-Cure Transition in Thalassemia Research: Semantic Topic Modeling of 17,651 Publications Across Three Decades.

Uncovering the True Genotype: Unusually Severe Sickle Cell Disease in a Child with an Initial HbSC Diagnosis.

Ocular Complications Among Patients with Beta-Thalassaemia Major and Intermedia: A Comparative Study from Pakistan.

Psychometric Performance of the Adult Sickle Cell Quality-of-Life Measurement Information System (ASCQ-Me) in Jamaicans with Sickle Cell Disease.

Co-Heredity of (-α)20.5 Deletion and IVS I-1 G > A (HBB: C.92 + 1 G > A) Mutations in a Pediatric Patient: A Cause of Moderate Anemia Phenotype?

A 21-Year Diagnostic Odyssey in TBC1D24-Associated Developmental and Epileptic Encephalopathy With Favorable Response to Corpus Callosotomy: A Case Report.

Male Goltz Syndrome due to Postzygotic PORCN Mosaicism: A Case Report.

Characterization of ntrk receptors and bdnf ligand in Cynoglossus semilaevis provides molecular insights into sexual size dimorphism regulation in flatfish.

Late diagnosis of Gitelman syndrome in an elderly patient: identification of a novel SLC12A3 pathogenic variant.

Sex-ratio distorters enable pre-zygotic sexing for sex-specific transcriptomics in Anopheles gambiae embryos.

Asymmetric Functional Divergence of alx4a and alx4b in Iridophore Differentiation and Cranial Development in Nile Tilapia.

Related Experiment Videos

Hb Madrid or alpha 2 beta (2)115(G17)Ala-->Pro in a black teenager

Related Concept Videos

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