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CYTOGENETICS IN MAN
NUMERICAL CONSIDERATIONS IN GENETICS
THE FAMILY PEDIGREE AND GENETIC
15 other sections not shown
aberrations abnormalities Addison's disease adrenal adult affected aldosterone Amer Amer.J amino acid anemia anomalies appear Arch artery associated ataxia atrial atrophy autosomal dominant autosomal recessive blood cardiac cells Chap characteristic chromosome chronic clinical condition congenital cystic deafness decreased defect deficiency described diabetes diagnosis disease disorder drome dystrophy Ehlers-Danlos syndrome enzyme erythrocyte factors females fetal fetal hemoglobin fibrosis frequently gene genetic genitalia glands globin gonadal gonadal dysgenesis heart hemo hemoglobin hemoglobin A2 hereditary heritable hormone hyper hypercalcemia hyperplasia hypertension hypoparathyroidism hypothyroidism incidence increased individuals inheritance involvement lesions males manifestations Marfan's syndrome metabolism muscle muscular mutation Neurol neurological normal occur onset parathyroid parents pathological patients percent phenotypic pheochromocytoma pituitary plasma present primary protein pulmonary renal reported result serum siblings skin somal stenosis studies suggested symptoms syndrome synthesis thalassemia thyroid tion tissue trait tuberous sclerosis tumors Turner's syndrome urinary urine usually ventricular X-linked