Professor Medical Genetics and Pediatrics, retired
Medical Genetics
Dr. Everett W. Lovrien, MD
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Everett Lovrien practices Medical Genetics. He went to medical school at University of Minnesota Medical School. University of Minnesota Medical School is ranked 40/10 in Research/PrimaryCare. Doctor Everett W. Lovrien, MD is also published. He has 72 publications published. The lastest publication: "Human centromere mapping using teratoma data.'
Publications
- SYMPOSIUM: BATTERED CHILD SYNDROME.
- GRAND ROUNDS: IDIOPATHIC HYPERCALCEMIA.
- GRAND ROUNDS: HASHIMOTO''S THYROIDITIS.
- Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA.
- A second gene for cerulean cataracts maps to the beta crystallin region on chromosome 22.
- AIDS-associated non-Hodgkin's lymphomas as primary and secondary AIDS diagnoses in hemophiliacs. Hemophilia Malignancy Study Group.
- Acquired immunodeficiency syndrome-associated non-Hodgkin's lymphomas and other malignancies in patients with hemophilia.
- A locus for the nystagmus-associated form of episodic ataxia maps to an 11-cM region on chromosome 19p.
- Familial periodic ataxia.
- Translocation(X;Y)(p22.33;p11.2) in XX males: etiology of male phenotype.
- Management of fractures in hemophilia.
- Recurrent sepsis with deficiencies of C2 and galactokinase.
- Linkage analysis in dominant optic atrophy.
- Familial cutaneous malignant melanoma: autosomal dominant trait possibly linked to the Rh locus.
- Chromosome heteromorphism analysis in cases of disputed paternity.
- Alpha-1-antitrypsin protease inhibitor (Pi) phenotypes in Down''s syndrome patients and their parents.
- Linkage analysis in lattice corneal dystrophy.
- Alteration of T-lymphocyte subpopulations in children, youth and adults with hemophilia A.
- Resolution of breakpoints in a complex rearrangement by use of multiple staining techniques: confirmation of suspected 12p12.3 intraband by deletion dosage effect of L...
- Genetic diagnosis in the newborn. A part of preventive medicine.
- Heritable fragile site on chromosome 16: probable localization of haptoglobin locus in man.
- Unusual dental findings in a patient with a rare bone dysplasia (dyschondrosteosis) and a chromosomal anomaly.
- Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+).
- Juvenile sex-linked retinoschisis: clinical and genetic studies.
- Mosaicism with translocation: autoradiographic and fluorescent studies of an inherited reciprocal translocation t(2q+;14q-).
- Chromosomal localization of the heterochromatic region 16qh(.76) linked to alpha-haptoglobin in man.
- Hemoglobin Casper: beta 106 (G8) Leu leads to Pro; a contemporary mutation.
- Human amylase loci: genetic linkage with the Duffy blood group locus and assignment to linkage group I.
- The nephropathy of the nail-patella syndrome. Clinicopathologic analysis of 11 kindred.
- Probable genetic linkage between human serum amylase (Amy 2 ) and Duffy blood group.
- A mother with Down''s syndrome and her chromosomally normal infant.
- Nonrandomness of translocations in man: preferential entry of chromosomes into 13-15-21 translocations.
- Haemopexin in human serum: a search for genetic polymorphosm.
- Tandem duplication of proximal 22q: a cause of cat-eye syndrome.
- Human chromosome variation: the discriminatory power of Q-band heteromorphism (variant) analysis in distinguishing between individuals, with specific application to ca...
- Hereditary melanoma, the dysplastic nevus syndrome, and transferrin.
- Inherited C3 deficiency with recurrent infections and glomerulonephritis.
- Factor IXPortland: a nonsense mutation (CGA to TGA) resulting in hemophilia B.
- Molecular genetics of human blue cone monochromacy.
- Structural and functional basis of the developmental regulation of human coagulation factor IX gene: factor IX Leyden.
- Microphthalmos in the presumed homozygous offspring of a first cousin marriage and linkage analysis of a locus in a family with autosomal dominant cerulean congenital ...
- Cosegregation of elastin-associated microfibrillar abnormalities with the Marfan phenotype in families.
- Oral motor dysfunction in individuals at risk of Huntington disease.
- CG dinucleotide transitions in the factor IX gene account for about half of the point mutations in hemophilia B patients: a Seattle series.
- Diffuse capillary hemangiomas associated with skeletal hypotrophy.
- Dyschondrosteosis and Madelung''s deformity. Report of three kindreds and review of the literature.
- Linkage relations of the loci for the MN blood group and red cell acid phosphatase.
- Linkage relationships of 1qh to Amy, Fy, PGM1, and Rh.
- Linkage group I: multipoint mapping.
- Exclusion gene mapping utilizing patients with chromosome imbalance: the HL-A system as a prototype.
- Gene dosage: evidence for assignment of erythrocyte acid phosphatase locus to chromosome 2.
- The linkage and mapping relationships of 1qh.
- Linkage group I: the simultaneous estimation of recombination and interference.
- Further evidence for the assignment of the red cell acid phosphatase gene (ACP1) to the short arm of chromosome 2 from gene dosage effect.
- Estimating distances from the centromere by means of benign ovarian teratomas in man.
- Human centromere mapping using teratoma data.
- Ovarian teratomas: cytologic data.
- The linkage and mapping relationships of 1 qh.
- Mannosidosis in three brothers--a review of the literature.
- Exclusion of glutathione reductase from 8pter leads to 8p22 and localization to 8p21.
- Linkage relationships of HLA and a familial chromosome 6 inversion (pter leads to p23::q23 leads to qter): lack of dose effect in duplication-deficient offspring.
- Linkage relationships of dominant antithrombin III deficiency and the heterochromatic region of chromosome 1.
- Serum cholinesterase (E2) linkage analysis: possible evidence for localization to chromosome 16.
- Linkage study of antithrombin III.
- Human benign ovarian teratomas: chromosomal and electrophoretic enzyme studies.
- Chorioangioma of the placenta and intrauterine growth failure.
- Central nervous system arteriovenous malformations in multiple generations of a family with hereditary hemorrhagic telangiectasia.
- The 8p- syndrome.
- Aicardi''s syndrome. Case report, clinical features, and electrophysiologic studies.
- The fetal trimethadione syndrome: report of an additional family and further delineation of this syndrome.
- Parental origin of the extra chromosome in Down''s syndrome.
Schools
University of Mn Med Sch
Doctors Specialties
- Clinical Genetics
- Pediatrics
- Medical Genetics
Accepted Insurances
Education
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Stanford University -
Children's National Medical Center - George Washington University -
University of California San Diego -
University of Minnesota Medical School
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