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Genetics Lab Publications


  • The Activity Degress of Trimethoprisul-Phamethoxazol in the Serum of Normal People.


  • Study Of Tumor Antigens In Rabbits Induced By " Myxoma Virus" And The Treatment Of The Tumor With BCG Vaccine.


  • In-Vitro Determination Of Cellular Immune Response: Studies On Macrophages Migration Inhibition Test With Human Lymphocytes.
  • Study Of Immune Response At T And B Level.


  • Studies On Heart Reactive Antibodies In Rheumatic Fever,  By Immunofluorescence Antibody Technique.


  • Investigation Of Immune System To Heptenic Molecules.
  • Studies On Heart Reactive Antibodies In Rheumatic Fever.
  • Comparison Of Specificities Of Hormonal And Cellular Immune Response To Hepatens.


  • Induction Of T-Cell Response To Herptens Coupled To Mycobacteria.


  • Clinical Trail Of Trophical Disodium Chromoglycate In Vernal Keratoconjuctivitis.


  • Tosson A, Morsy SM, El-Khateeb M: The Prevalence Of Some Parasites In Students Of Jordan University. J. Egy. Soc. Parasito. 9, 495, 1979.


  • Study Of Toxoplasma Antibodies In Jordanian Adults.
  • The Effect Of Glucose On Growth Hormone Response To Diazepam.
  • The Effect Of Acute Hypercalcemia On Prolactin Release In Man.
  • Thyroid Disorders In Jordan ( Clinical And Etiological Review ).
  • Serum Protein Values In Healthy Jordanian Mothers And Their Neonates.
  • Hyperthroidism In Jordan,  A Clinical And Aetiological Review.


  • Thyroid Disorders In Jordan.
  • Renal Amyloidosis .
  • Lactose Malabsorption In Jordanian Infants And Children.


  • The Response Of Growth Hormone And Prolactin To Oral Diazepam In Diabetics .


  • •    Seroimmnity To Rubella Virus In Jordanians.
  • •    Therapeutic Effect Of Vincristine, Adriamycin And Predinsolone  (Vap) In Angioimmunoblastic Lymphadenopathy.
  • •    Therapeutic effect of vincristine, adriamycin and prednisolone (VAP) in angioimmunoblastic lymphadenopathy (AIL).


  • Serum Ferritin In Evaluation Of Iron Status In Children.
  • Hydroxylase  Deficiency  With Pulmonary Stenosis And Skeletal Abnormalities.
  • Cure Rate Of Burkitts Lymphoma In Jordanian Children With Multiple Drug Chemotherapy.


  • Immunological Parameters In Institutionalized Mentally Retarded And Non-Institutionalized Healthy Children.


  • HLA Antigens Blood Groups And Immunoglublin  Levels In Idiopathic  Thrombocytopenic Purpura 5 Th Int Cong.
  • Hepatitis B Virus And HTLVI-II Antibodies In Patients With Bleeding Disorders In Jordan.
  • HLA Antigens, Blood Groups, And Immunoglobulin Levels In Idiopathic  Thrombocytopenic Purpura.
  • A Control Trait Of Steroid And Splenectomy Of Adult Idiopathic Thrombocytopenic Purpura.
  • Burkitts Lymphoma In Jordanian Children; Epidemiological And Clinical Study.
  • Barkits Lymphoma In Jordan.


  • Incidence Of Antibodies To Epstein-Barr Virus In Jordanian Partients With Lympho- Proliferative Diseases.


  • Serological Assessments Of Streptoccoccal  Infection By Comparison Of Antibody Titers To Streptococcal Extracellular Antigens.
  • Incidence Of HIV Antibodies In Jordan
  • An Improved Method For The Preparation Of  Ploy (Adenosine- Diphosphate -Ribsone ) With Twenty Units Lenght Chain.
  • IgA Nephropathy In Patients With Familial Mediterranean Fever.


  • Comparison Of Antibody Titers To Streptoccocal Extracellular Antigens.
  • Rapid Progressive Glomerulonephritis In Patients With Familial Mediterranean Fever.
  • Effects Of Aflatoxin B1 On Serum And  Pituitary Prolaction Levels In Male Rates.


  • Diagnosis And Treatment Of 106 Prospective Cases Of Human  Brucellosis Of Infection.


  • Comparison Of Four Methods For The Detction Of Cytomegalovirus Antibodies And The Prevalence Of Cytomegalovirus Antibodies Among Jordanian Blood Donors.
  • Hepatitis-B Markers In Patients With Bleeding Disorders.
  • HLA-Antigne And  Estrogen Receptors In Breast Cancer.


  • Arginine - Vasopressin And Endothelial Associated Protein In Thyroid Disease.
  • Spectrum of renal involvement in familial Mediterranean fever.


  • The Prevalence Thyroid Function Tests In Rheumatic Diseases.
  • Autosomal recessive ataxia, slow eye movements and psychomotor retardation.
  • Smith - Magenis Syndrome : Unreported Findings And Review Of The Literature.
  • Effect Of Nigella Sativa Volatile Oil On Jukat T Cell Leukemia Cell Line Polypeptiodes.


  • Multiple Sclerosis In Arab Jordanians.
  • LDH activity in pediatric none tumoral hydrocephalus.
  • Serodiagnosis of cutaneous leishmaniasis in Jordan using indirect fluorescent antibody test and the enzyme-linked immunosorbent assay.


  • Epidemiology Of Multiple Sclerosis In Arabs In Jordan: A  Comparative Study Between Jordanians And Palestinians.


  • Characterization of Beta - Globin gene mutations in Jordanians.
  • Prenatal Diagnosis, Genetic Laboratory Experience.


  • Clinical and genetic heterogeneity of Wolfram syndrome.


  • A nonsense in the retinal specific guanylate cyclase gene is the cause of Leber congenital amaurosis in a large inbred kindred from Jordan.
  • A case of Wolfram Syndrome in Triplets: Some Newly Recognized Features.
  • Distal hereditary motor neuronopathy of the Jerash type.
  • Humoral response of Meriones libycus to experimental infection with Leishmania major.
  • The identification of a second Wolfram syndrome locus: Further evidence of locus heterogeneity.


  • A Noval Form Of Distal Hereditary Motor Neuronopathy (HMN-J) Maps To Chromosome 9p21.1-P12.
  • Homozygosity Mapping Identifies an Additional Locus for Wolfram Syndrome on Chromosome  4q.
  • Familial disorder of sex determination in seven individuals from three related sibships.
  • Validation Studies Of Random Amplified Polymorphic Dna (Rapd) In Human And The Possibility Of Its Implementation In Forensic.


  • The Prvalenceof Hepatitis B, Hepatitis C And Human Immunodeficiency Virus Markers In Multi Transfuse Patients.


  • Genotype/phenotype correlations in Arab patients with familial Mediterranean fever.
  • Wolfram Syndrome: Identification of a phenotypic and Genotypic Variant from Jordan.
  • Thyroid Function and Thyroid Autoimmunity in Patients with Type 1 Diabetes Mellitus.
  • Effects of Short term Metformin Administration on Androgens in Normal Men.
  • Cerebellar Hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, phsychomotor retardation and short stature:”D-CHRAMPS Syndrome”.


  • Epidemiology and management of hypertension among Bedouins in Northern Jordan.
  • Familial Mediterranean fever mutation frequencies and carrier rates among a mixed Arabic population.
  • Antibodies to Glutamic Acid Decarboxylase in Syrian and Jordanian Type 1 diabetes patients and their siblings.
  • Alopecia universalis congenital, XY gonadal dysgenesis and laryngomalacia: a novel malformation syndrome.
  • Thyroid function and thyroid autoimmunity in patients with type 1 diabetes mellitus.


  • Thyroid dysfunction in patients with type 2 diabetes mellitus in Jordan.


  • The spectrum of familial Mediterranean fever gene mutations in Arabs: report of a large series.
  • Wrinkly Skin Syndrome.
  • Cockayne Syndrome in 2 siblings.


  • •    Familial mediterranean fever in Arabs.
  • •    Importance of rotavirus as a cause of gastroenteritis in Jordan: a hospital based study.
  • •    Familial Mediterranean fever in the Syrian population: gene mutation frequencies, carrier rates and phenotype-genotype correlation.
  • •    Brachydactyly type B1: report o a family with de Novo ROR2 mutation.
  • •    Etiological and consanguinity profiles of disorders referred to a genetic counselling clinic in Jordan.


  • High prevalence of the metabolic syndrome among Northern Jordanians.
  • Successful bone marrow transplantation for treatment of chronic myeloid leukemia from a donor with mosaic Klinefelter syndrome.
  • A Homozygous Mutation in a Novel Zinc-Finger Protein, ERIS, Is Responsible for Wolfram Syndrome.
  • Consanguinity and genetic disorders. Profile from Jordan.
  • Jordan: Communities and community genetics.
  • Cenani– Lenz syndactyly with facial dysmorphism, hypothyroidism, and renal hypoplasia: a case report.


  • An increase in prevalence of diabetes mellitus in Jordan over 10 years.
  • Prevalence of sexually transmitted infections among sexually active Jordanian females.
  • Obesity in Jordan: prevalence, associated factors, comorbidities, and change in prevalence over ten years.
  • The transforming mutation E17K/AKT1 is not a major event in B-cell-derived lymphoid leukaemias.


  • First Report of Clinical, Functional, and Molecular Investigation of Chronic Granulomatous Disease in Nine Jordanian Families.
  • Β-Thalassemia: Prevention in Jordan. PDF


  • The prevelance of FMR1 premutation/full mutation in Jordanian patients with cognitive impairments, mental retardation, or premature ovarian insufficiency (POI). PDF


  • Depression is associated with low levels of 25-hydroxyvitamin D among Jordanian adults: results from a national population survey.
  • Hypertension prevalence, awareness, treatment and control, and associated factors: results from a national survey, jordan.
  • Identification of the most common mutations in the Phenylalanine Hydroxylase (PAH) gene in Jordanian Patients. PDF
  • Prevelance of Congenital Adrenal Hyperplasia (CAH) due to 21-Hydroxylase deficiency in a Jordanian Sample Pool. PDF


  • Study of Turner Syndrome and Presentation of unique cases in the Jordanian population. PDF