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Items: 1 to 50 of 56

1.

Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA.

Litt M, Kramer P, LaMorticella DM, Murphey W, Lovrien EW, Weleber RG.

Hum Mol Genet. 1998 Mar;7(3):471-4.

PMID:
9467006
2.

AIDS-associated non-Hodgkin's lymphomas as primary and secondary AIDS diagnoses in hemophiliacs. Hemophilia Malignancy Study Group.

Ragni MV, Belle SH, Jaffe R, Locker J, Duerstein SL, Bass DC, Addiego JE, Aledort LM, Barron LE, Brettler DB, Buchanan GR, Gill JC, Ewenstein BM, Green D, Hilgartner MW, Hoots WK, Kisker CT, Lovrien EW, Rutherford CJ, Sanders NL, Smith KJ, Stabler SP, Swindells S, White GC 3rd, Kingsley LA.

J Acquir Immune Defic Syndr Hum Retrovirol. 1996 Sep;13(1):78-86.

PMID:
8797689
3.

Acquired immunodeficiency syndrome-associated non-Hodgkin's lymphomas and other malignancies in patients with hemophilia.

Ragni MV, Belle SH, Jaffe RA, Duerstein SL, Bass DC, McMillan CW, Lovrien EW, Aledort LM, Kisker CT, Stabler SP, et al.

Blood. 1993 Apr 1;81(7):1889-97.

4.

Diffuse capillary hemangiomas associated with skeletal hypotrophy.

Beals RK, Lovrien EW.

J Pediatr Orthop. 1992 May-Jun;12(3):401-2.

PMID:
1573010
5.
6.
7.

Structural and functional basis of the developmental regulation of human coagulation factor IX gene: factor IX Leyden.

Hirosawa S, Fahner JB, Salier JP, Wu CT, Lovrien EW, Kurachi K.

Proc Natl Acad Sci U S A. 1990 Jun;87(12):4421-5.

8.

Factor IXPortland: a nonsense mutation (CGA to TGA) resulting in hemophilia B.

Chen SH, Scott CR, Schoof J, Lovrien EW, Kurachi K.

Am J Hum Genet. 1989 Apr;44(4):567-9.

10.

Tandem duplication of proximal 22q: a cause of cat-eye syndrome.

Reiss JA, Weleber RG, Brown MG, Bangs CD, Lovrien EW, Magenis RE.

Am J Med Genet. 1985 Jan;20(1):165-71.

PMID:
3970068
11.

Linkage analysis in lattice corneal dystrophy.

Kivlin JD, Lovrien EW, Maumenee IH, Bishop DT, Bias W.

Am J Med Genet. 1984 Oct;19(2):387-90.

PMID:
6334443
12.

Alteration of T-lymphocyte subpopulations in children, youth and adults with hemophilia A.

Wolff LJ, Borzy M, Kamoun M, Lovrien EW.

Scand J Haematol Suppl. 1984;40:375-7. No abstract available.

PMID:
6332374
13.

Linkage analysis in dominant optic atrophy.

Kivlin JD, Lovrien EW, Bishop DT, Maumenee IH.

Am J Hum Genet. 1983 Nov;35(6):1190-5.

14.

Chromosome heteromorphism analysis in cases of disputed paternity.

Olson SB, Magenis RE, Rowe SI, Lovrien EW.

Am J Med Genet. 1983 May;15(1):47-55.

PMID:
6574701
15.

Management of fractures in hemophilia.

Wolff LJ, Lovrien EW.

Pediatrics. 1982 Sep;70(3):431-6.

PMID:
6810299
16.

Alpha-1-antitrypsin protease inhibitor (Pi) phenotypes in Down's syndrome patients and their parents.

Bufton L, Magenis RE, Lovrien EW.

Clin Genet. 1982 Jan;21(1):14-8.

PMID:
6461441
17.

Familial periodic ataxia.

Margolin DI, Nutt JG, Lovrien EW.

Trans Am Neurol Assoc. 1981;106:53-7. No abstract available.

PMID:
7349006
18.

The 8p- syndrome.

Reiss JA, Brenes PM, Chamberlin J, Magenis RE, Lovrien EW.

Hum Genet. 1979 Mar 12;47(2):135-40.

PMID:
437781
19.

Chorioangioma of the placenta and intrauterine growth failure.

King CR, Lovrien EW.

J Pediatr. 1978 Dec;93(6):1027-8. No abstract available.

PMID:
722419
20.

Aicardi's syndrome. Case report, clinical features, and electrophysiologic studies.

Weleber RG, Lovrien EW, Isom JB.

Arch Ophthalmol. 1978 Feb;96(2):285-90.

PMID:
415707
21.

Linkage relationships of dominant antithrombin III deficiency and the heterochromatic region of chromosome 1.

Magenis RE, Donlon T, Parks M, Rivas ML, Lovrien EW.

Cytogenet Cell Genet. 1978;22(1-6):327-9. No abstract available.

PMID:
752496
22.

Serum cholinesterase (E2) linkage analysis: possible evidence for localization to chromosome 16.

Lovrien EW, Magenis RE, Rivas ML, Lamvik N, Rowe S, Wood J, Hemmerling J.

Cytogenet Cell Genet. 1978;22(1-6):324-6. No abstract available.

PMID:
752495
23.

Linkage study of antithrombin III.

Lovrien EW, Magenis RE, Rivas ML, Goodnight S, Moreland R, Rowe S.

Cytogenet Cell Genet. 1978;22(1-6):319-23. No abstract available.

PMID:
752494
24.

Human benign ovarian teratomas: chromosomal and electrophoretic enzyme studies.

Patil SR, Kaiser-McCaw B, Hecht F, Linder D, Lovrien EW.

Birth Defects Orig Artic Ser. 1978;14(6B):297-301. No abstract available.

PMID:
728570
25.
26.

The fetal trimethadione syndrome: report of an additional family and further delineation of this syndrome.

Feldman GL, Weaver DD, Lovrien EW.

Am J Dis Child. 1977 Dec;131(12):1389-92.

PMID:
412416
27.

Mannosidosis in three brothers--a review of the literature.

Vidgoff J, Lovrien EW, Beals RK, Buist NR.

Medicine (Baltimore). 1977 Jul;56(4):335-48.

PMID:
875720
28.

Estimating distances from the centromere by means of benign ovarian teratomas in man.

Ott J, Linder D, McCaw BK, Lovrien EW, Hecht F.

Ann Hum Genet. 1976 Nov;40(2):191-6.

PMID:
1015813
29.

Dyschondrosteosis and Madelung's deformity. Report of three kindreds and review of the literature.

Beals RK, Lovrien EW.

Clin Orthop Relat Res. 1976 May;(116):24-8.

PMID:
1277646
30.

The linkage and mapping relationships of 1qh.

Rivas ML, Conneally PM, Lovrien EW, Magenis RE, Merritt AD, Meyers DA, Palmer CG, Parks M, Wang L, Yu PL.

Birth Defects Orig Artic Ser. 1976;12(7):347-50. No abstract available.

PMID:
1024639
31.

Linkage group I: the simultaneous estimation of recombination and interference.

Meyers DA, Conneally PM, Lovrien EW, Magenis RE, Merritt AD, Norton JA, Palmer CG, Rivas ML, Wang L, Yu PL.

Birth Defects Orig Artic Ser. 1976;12(7):335-9. No abstract available.

PMID:
1024636
32.

Human centromere mapping using teratoma data.

Ott J, Hecht F, Linder D, Lovrien EW, Kaiser B, McCaw BK.

Cytogenet Cell Genet. 1976;16(1-5):96-8. No abstract available.

PMID:
975932
33.

Ovarian teratomas: cytologic data.

McCaw BK, Hecht F, Linder D, Lovrien EW, Wyandt H, Bacon D, Clark B, Lea N.

Cytogenet Cell Genet. 1976;16(1-5):391-5. No abstract available.

PMID:
975915
34.

The linkage and mapping relationships of 1 qh.

Rivas ML, Conneally PM, Lovrien EW, Magenis RE, Merritt AD, Meyers DA, Palmer CG, Parks M, Wang L, Yu PL.

Cytogenet Cell Genet. 1976;16(1-5):347-50. No abstract available.

PMID:
975906
35.

Linkage group I: the simultaneous estimation of recombination and interference.

Meyers DA, Conneally PM, Lovrien EW, Magenis RE, Merritt AD, Norton JA, Palmer CG, Rivas ML, Wang L, Yu PL.

Cytogenet Cell Genet. 1976;16(1-5):335-9. No abstract available.

PMID:
975904
36.

Human centromere mapping using teratoma data.

Ott J, Hecht F, Linder D, Lovrien EW, McCaw BK.

Birth Defects Orig Artic Ser. 1976;12(7):396-8.

PMID:
799523
37.

Ovarian teratomas: cytologic data.

McCaw B, Hecht F, Linder D, Lovrien EW, Wyandt H, Bacon D, Clark B, Lea N.

Birth Defects Orig Artic Ser. 1976;12(7):391-5. No abstract available.

PMID:
66945
38.

Linkage relations of the loci for the MN blood group and red cell acid phosphatase.

Weitkamp LR, Lovrien EW, Olaisen B, Fenger K, Gedde-Dahl T Jr, Sorensen SA, Conneally PM, Bias WB, Ott J.

Birth Defects Orig Artic Ser. 1975;11(3):276-80. No abstract available.

PMID:
1203495
39.

Linkage relations of the loci for the MN blood group and red cell acid phosphatase.

Weitkamp LR, Lovrien EW, Olaisen B, Fenger K, Gedde-Dahl T Jr, Sorensen SA, Conneally PM, Bias WB, Ott J.

Cytogenet Cell Genet. 1975;14(3-6):446-50. No abstract available.

PMID:
1192835
40.

Linkage relationships of 1qh to Amy, Fy, PGM1, and Rh.

Rivas ML, Conneally PM, Hecht F, Lovrien EW, Magenis E, Merritt AD, Meyers DA, Palmer CG, Wang L.

Cytogenet Cell Genet. 1975;14(3-6):409-17. No abstract available.

PMID:
1192828
41.

Linkage group I: multipoint mapping.

Meyers DA, Conneally PM, Hecht F, Lovrien EW, Magenis E, Merritt AD, Palmer GC, Rivas ML, Wang L.

Cytogenet Cell Genet. 1975;14(3-6):381-9. No abstract available.

PMID:
1192823
42.

Linkage relationships of 1qh to Amy, Fy, PGM1, and Rh.

Rivas ML, Conneally PM, Hecht F, Lovrien EW, Magenis E, Merritt AD, Meyers DA, Palmer CG, Wang L.

Birth Defects Orig Artic Ser. 1975;11(3):239-47. No abstract available.

PMID:
812569
43.

Linkage group I: multipoint mapping.

Meyers DA, Conneally PM, Hecht F, Lovrien EW, Magenis E, Merritt AD, Palmer CG, Rivas ML, Wang L.

Birth Defects Orig Artic Ser. 1975;11(3):211-9. No abstract available.

PMID:
812567
44.

Human amylase loci: genetic linkage with the Duffy blood group locus and assignment to linkage group I.

Merritt AD, Lovrien EW, Rivas ML, Conneally PM.

Am J Hum Genet. 1973 Sep;25(5):523-38. No abstract available.

45.

The nephropathy of the nail-patella syndrome. Clinicopathologic analysis of 11 kindred.

Bennett WM, Musgrave JE, Campbell RA, Elliot D, Cox R, Brooks RE, Lovrien EW, Beals RK, Porter GA.

Am J Med. 1973 Mar;54(3):304-19. No abstract available.

PMID:
4569963
46.

Mosaicism with translocation: autoradiographic and fluorescent studies of an inherited reciprocal translocation t(2q+;14q-).

Reiss JA, Wyandt HE, Magenis RE, Lovrien EW, Hecht F.

J Med Genet. 1972 Sep;9(3):280-6. No abstract available.

47.

Probable genetic linkage between human serum amylase (Amy 2 ) and Duffy blood group.

Hill CJ, Rowe SI, Lovrien EW.

Nature. 1972 Jan 21;235(5334):162-3. No abstract available.

PMID:
4551225
48.

Chromosomal localization of the heterochromatic region 16qh(.76) linked to alpha-haptoglobin in man.

Hecht F, Tolby B, Magenis RE, Kimberling WJ, Wyandt H, Lovrien EW.

Nature. 1971 Oct 15;233(5320):480. No abstract available.

PMID:
4939541
49.

Unusual dental findings in a patient with a rare bone dysplasia (dyschondrosteosis) and a chromosomal anomaly.

Stewart RE, Lovrien EW, Wyandt HE.

Oral Surg Oral Med Oral Pathol. 1971 Oct;32(4):596-604. No abstract available.

PMID:
5285697
50.

Juvenile sex-linked retinoschisis: clinical and genetic studies.

Burns RP, Lovrien EW, Cibis AB.

Trans Am Acad Ophthalmol Otolaryngol. 1971 Sep-Oct;75(5):1011-21. No abstract available.

PMID:
5097816

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