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973 results on '"Siobhan D. Ma"'

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901. Arrhythmias in Acute Myocardial Infarction

902. APC Resistance

903. Ménétrier's Disease

904. Autoimmune Myasthenia Gravis

905. Milk Alkali Syndrome

906. Amaurosis, Leber Congenital

907. Aggressive NK Cell Leukemia

908. Argininosuccinic Acid Synthetase Deficiency

909. Acid β-Glucosidase Deficiency

910. Epilepsy, Benign Childhood with Centrotemporal Spikes and other Idiopathic Partial Epilepsies of Childhood

911. Autosomal Dominant Mandibulofacial Dysostosis

912. Membranous Glomerulonephritis

913. Achalasia

914. Mohr-Wreidt Type Brachydactyly

915. α-1 Antitrypsin Deficiency

916. Macular Dystrophy, Best’s Vitelliform

917. Anhidrotic Ectodermal Dysplasia with Immunodeficiency, Osteopetrosis and Lymphedema

918. Attention-Deficit Disorder

919. Meige Lymphedema

920. Edwards Syndrome

921. Episodic Ataxia Type 1 and Type 2

922. Muscular Dystrophy, Emery-Dreifuss, X-linked

923. Elevated Factor XI Level

924. Esophagitis, Eosinophilic

925. ADD

926. Adrenomyeloneuropathy

927. Malignant Hyperpyrexia

928. Atopic Eczema

929. Melkersson-Rosenthal Syndrome

930. Early Onset Breast-ovarian Cancer Syndrome

931. Respiratory Acidosis

932. Atypical HUS

933. Right and Left Isomerism

934. Empyema

935. Mongolian Spots

936. Arthritis, Infectious

937. Autoimmune Inner Ear Disease

938. Androgenetic Alopecia

939. Rotor Syndrome

940. Actinic Keratosis

941. Myopia: Molecular Targets and Gene Mapping Attempts

942. Mild Hyperphenylalaninemia

943. AFLD

944. Multiple Symmetric Lipomatosis

945. Renal Hypouricemia, Hereditary

946. RCDP Type 3

947. Rod Monochromatism

948. Myotonic Dystrophy Type 1

949. ADA-deficient Severe Combined Immune Deficiency (ADA-SCID)

950. Actinic Keratosis and Squamous Cell Carcinoma

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