Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Consanguinity, the driving force behind inheritance of HbS-β thalassemia in Southern Districts of KP.

JPMA. The Journal of the Pakistan Medical Association - 1 Jun 2020

Khan Jabbar, Muhammad Dost, Ismail Muhammad, Khan Inamullah, Niaz Shahid

Abstract excerpt

OBJECTIVE: To determine the clinical, haematological and genetic factors responsible for variable phenotypes of sickle haemoglobin, sickle haemoglobin-beta, and beta-thalassemia patients. METHODS: The study was conducted in Bannu, Lakki, Tank and Dera Ismail Khan districts of Khyber Pakhtunkhwa province of Pakistan from September 2016 to November 2017, and comprised sickle haemoglobin, sickle haemoglobin-beta,...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to alpha-Thalassemia
Share to beta-Thalassemia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Consanguinity

Share to DNA Mutational Analysis

Share to Mutation

Share to Pakistan

Source

Identifiers

PMID: 32810090
DOI: 10.5455/JPMA.300622

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Consanguinity, the driving force behind inheritance of HbS-β thalassemia in Southern Districts of KP.PMID 32810090Read ↗

Genetic basis of ß-thalassemia in families of pashtun ethnicity in Dera Ismail Khan district of Khyber Pakhtun-Khwa province, Pakistan.Semantic proximity Read ↗

Exploring the role of consanguinity in thalassemia prevalence in Pakistan: an in-depth analysis of genetic and cultural factors affecting public healthSemantic proximity Read ↗

Thalassemia: Impact of consanguineous marriages on most prevalent monogenic disorders of humansSemantic proximity Read ↗

Molecular Heterogeneity of β-Thalassemia in the Kohat Region, Khyber Pakhtunkhwa Province, Pakistan.Semantic proximity Read ↗

Genetic determinants of β-thalassemia intermedia in Pakistan.Semantic proximity Read ↗

Sickle cell disease in Middle East Arab countriesSemantic proximity Read ↗

Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western IndiaSemantic proximity Read ↗

The genetic architecture of the β-globin chain in individuals with and without sickle cell disease in Nigeria: A case for beta thalassemia?Semantic proximity Read ↗

Distribution of hemoglobinopathy disorders in Saudi Arabia based on data from the premarital screening and genetic counseling program, 2011–2015Semantic proximity Read ↗

Prevalence and Regional Distribution of Beta-Hemoglobin Variants in Saudi Arabia: Insights from the National Premarital Screening Program" Running Title: Burden of Beta-Globin Variants in Saudi ArabiaSemantic proximity Read ↗

Genetic diversity of beta-thalassemia mutations in Pakistani population.Semantic proximity Read ↗

Genetic patterns & public health implications of sickle cell anaemia across populations: A systematic review.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.