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HUMAN PHOSPHOGLYCOLATE PHOSPHATASE (PGP) E.C. 3.1.3.18: LINKAGE ANALYSISSIEBERT G; AMORIM A; KOEMPF J et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 3; PP. 421-423; BIBL. 5 REF.Article

Mitochondrial malic enzyme in human leukocytesSIEBERT, G; AMORIM, A.Human heredity. 1987, Vol 37, Num 2, pp 122-123, issn 0001-5652Article

Human erythrocyte pyrimidine 5'-nucleotidase isozymes : effect of sulfhydryl reagents and electrophoretic discriminationMANCO, L; AMORIM, A.Electrophoresis (Weinheim. Print). 1993, Vol 14, Num 10, pp 1084-1085, issn 0173-0835Article

Formal and population genetics of F13A and FUCA1 polymorphisms in Northern PortugalJOAO PRATA, M; AMORIM, A.Human heredity. 1990, Vol 40, Num 1, pp 45-48, issn 0001-5652Article

FORMAL GENETICS OF PHOSPHOGLYCOLATE PHOSPHATASE (PGP): INVESTIGATION ON 272 MOTHER-CHILD PAIRSAMORIM A; SIEBERT G; RITTER H et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 3; PP. 419-420; BIBL. 1 REF.Article

Genetic polymorphism of δ-aminolaevulinic acid dehydratase (E.C. 4.2.1.24, ALAD) in the domestic rabbitFERRAND, N; AMORIM, A.Animal genetics (Print). 1990, Vol 21, Num 2, pp 217-219, issn 0268-9146Article

Dynamics of microcystins in the mussel Mytilus galloprovincialisAMORIM, A; VASCONCELOS, V.Toxicon (Oxford). 1999, Vol 37, Num 7, pp 1041-1052, issn 0041-0101Article

AMINOLEVULINATE DEHYDRATASE (E. C. 4.2.1.24): LINKAGE ANALYSISAMORIM A; KOMPF J; SCHUNTER F et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 1; PP. 48-49; BIBL. 3 REF.Article

Y-chromosome STR haplotypes in East Timor : Forensic evaluation and population dataSOUTO, L; GUSMAO, L; FERREIRA, E et al.Forensic science international. 2006, Vol 156, Num 2-3, pp 261-265, issn 0379-0738, 5 p.Article

Genetic diversity of Y-specific STRs in chimpanzees (Pan troglodytes)GUSMAO, L; GONZALEZ-NEIRA, A; ALVES, C et al.American journal of primatology (Print). 2002, Vol 57, Num 1, pp 21-29, issn 0275-2565Article

Starfish acrosomal acid phosphatase: a cytochemical and biochemical studySOUSA, M; MORADAS FERREIRA, P; AMORIM, A et al.Biology of the cell. 1988, Vol 63, Num 1, pp 101-104, issn 0248-4900Article

Formal genetics of esterase D (EC 3.1.1.1): evidence for a sex-phenotype associationAMORIM, A; ROCHA, J; KÖMPF, J et al.Human heredity. 1988, Vol 38, Num 4, pp 255-257, issn 0001-5652Article

GRAVITY: a four-telescope beam combiner instrument for the VLTIGILLESSEN, S; EISENHAUER, F; BAUMEISTER, H et al.Proceedings of SPIE, the International Society for Optical Engineering. 2010, Vol 7734, issn 0277-786X, isbn 0-8194-8224-2 978-0-8194-8224-2, 2Vol, 77340Y.1-77340Y.20, 2Conference Paper

Do the distribution patterns of polymorphisms at the thiopurine S-methyltransferase locus in sub-Saharan populations need revision? Hints from Cabinda and MozambiqueOLIVEIRA, E; QUENTAL, S; ALVES, S et al.European journal of clinical pharmacology. 2007, Vol 63, Num 7, pp 703-706, issn 0031-6970, 4 p.Article

Population data on 15 autosomal STRs in a sample from East TimorSOUTO, L; ALVES, C; GUSMAO, L et al.Forensic science international. 2005, Vol 155, Num 1, pp 77-80, issn 0379-0738, 4 p.Article

Mitochondrial portrait of the Cabo Verde archipelago: the Senegambian outpost of Atlantic slave tradeBREHM, A; PEREIRA, L; BANDELT, H.-J et al.Annals of human genetics. 2002, Vol 66, Num 1, pp 49-60, issn 0003-4800Article

Haplotype analysis and phylogeny of ornithine transcarbamylase polymorphismsAZEVEDO, L; CALAFELL, F; VILARINHO, L et al.Annals of human genetics. 2002, Vol 66, Num 5-6, pp 379-385, issn 0003-4800, 7 p.Article

Two pairs of proven monozygotic twins discordant for familial amyloid neuropathy (FAP) TTR Met 30MUNAR-QUES, M; PEDROSA, J. L; COELHO, T et al.Journal of medical genetics. 1999, Vol 36, Num 8, pp 629-632, issn 0022-2593Article

β-amyloid precursor protein gene in squirrel monkeys with cerebral amyloid angiopathyLEVY, E; AMORIM, A; FRANGIONE, B et al.Neurobiology of aging. 1995, Vol 16, Num 5, pp 805-808, issn 0197-4580Article

Genetic polymorphism of human peptidase C, PEPC (E.C.3.4.1.1): formal genetic and population dataKÖMPF, J; PRATA, M. J; AMORIM, A et al.Human genetics. 1989, Vol 83, Num 2, pp 197-198, issn 0340-6717Article

Signatures of strong gravity with GRAVITYECKART, A; ZAMANINASAB, M; MUZIC, K et al.Proceedings of SPIE, the International Society for Optical Engineering. 2010, Vol 7734, issn 0277-786X, isbn 0-8194-8224-2 978-0-8194-8224-2, 2Vol, 77340X.1-77340X.11, 2Conference Paper

The Fiber Coupler subsystem of the future VLTI instrument GRAVITYPFUHL, O; EISENHAUER, F; STRAUBMEIER, C et al.Proceedings of SPIE, the International Society for Optical Engineering. 2010, Vol 7734, issn 0277-786X, isbn 0-8194-8224-2 978-0-8194-8224-2, 2Vol, 77342A.1-77342A.8, 2Conference Paper

Molecular mechanisms underlying large genomic deletions in ornithine transcarbamylase (OTC) geneQUENTAL, R; AZEVEDO, L; RUBIO, V et al.Clinical genetics. 2009, Vol 75, Num 5, pp 457-464, issn 0009-9163, 8 p.Article

Bantu and European Y-lineages in Sub-Saharan AfricaPEREIRA, L; GUSMAO, L; ALVES, C et al.Annals of human genetics. 2002, Vol 66, Num 5-6, pp 369-378, issn 0003-4800, 10 p.Article