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Publications by A S Teebi

Prenatal Diagnosis of Fragile X Syndrome: Identification of a Male Fetus Mosaic for a Premutation on Chorionic Villus Sampling - Management and Follow-Up

Genetics in Medicine
MedicineGenetics
2000English

Spondyloepiphyseal Dysplasia Tarda With Progressive Arthropathy: A Rare Disorder Frequently Diagnosed Among Arabs.

Journal of Medical Genetics
Genetics
1986English

Unusual Inheritance of Primary Ciliary Dyskinesia (Kartagener's Syndrome).

Journal of Medical Genetics
Genetics
1994English

New Autosomal Recessive Faciodigitogenital Syndrome.

Journal of Medical Genetics
Genetics
1988English

Profound Limb Deficiency, Thoracic Dystrophy, Unusual Facies, and Normal Intelligence: A New Syndrome.

Journal of Medical Genetics
Genetics
1985English

Osteoporosis-Pseudoglioma Syndrome With Congenital Heart Disease: A New Association.

Journal of Medical Genetics
Genetics
1988English

Meckel Syndrome and Neural Tube Defects in Kuwait.

Journal of Medical Genetics
Genetics
1992English

Complex Translocation Involving Chromosomes Y, 1, and 3 Resulting in Deletion of Segment 3q23----Q25.

Journal of Medical Genetics
Genetics
1986English

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