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Multiple common fragile sites are expressed in the genome of the laboratory ratROBINSON, T. J; ELDER, F. F. B.Chromosoma (Berlin. Print). 1987, Vol 96, Num 1, pp 45-49, issn 0009-5915Article

The chromosomes of Sigmodon ochrognathus and S. Fulviventer suggest a realignment of Sigmodon species groupsELDER, F. F. B; LEE, M. R.Journal of mammalogy. 1985, Vol 66, Num 3, pp 511-518, issn 0022-2372Article

Cytogenetics : its role in wildlife management and the genetic conservation of mammalsROBINSON, T. J; ELDER, F. F. B.Biological conservation. 1993, Vol 63, Num 1, pp 47-51, issn 0006-3207Article

Rodent common fragile sites: are they conserved: evidence from mouse and ratELDER, F. F. B; ROBINSON, T. J.Chromosoma (Berlin. Print). 1989, Vol 97, Num 6, pp 459-464, issn 0009-5915Article

Abnormality of platelet size and T-lymphocyte proliferation in an autosomal recessive form of dyskeratosis congenitaJUNEJA, H. S; ELDER, F. F. B; GARDNER, F. H et al.European journal of haematology. 1987, Vol 39, Num 4, pp 306-310, issn 0902-4441Article

Chromosomal evolution in the vlei rat, Otomys irroratus (Muridae : Otomyinae) : a compound chromosomal rearrangement separates two major cytogenetic groupsRAMBAU, R. V; ELDER, F. F. B; ROBINSON, T. J et al.Cytogenetics and cell genetics. 2001, Vol 93, Num 3-4, pp 253-257, issn 0301-0171Conference Paper

Acute monoblastic leukemia with a single chromosomal rearrangement involving break-points on chromosomes 8 and 16, 46, XX, t(8; 16) (p11; p13)JUNEJA, H. S; ELDER, F. F. B; RAJARAMAN, S et al.Acta haematologica. 1987, Vol 78, Num 1, pp 1-5, issn 0001-5792Article

Identification of abnormal chromosomal complement in formalin-fixed, paraffin-embedded placental tissueCOWLES, T. A; ELDER, F. F. B; TAYLOR, S et al.Prenatal diagnosis. 1995, Vol 15, Num 1, pp 21-26, issn 0197-3851Article

Evolution of chromosomal variation in cottontails, genus Sylvilagus (mammalia: Lagomorpha). II. Sylvilagus audubonii, S. idahoensis, S. nuttallii and S. palustrisROBINSON, T. J; ELDER, F. F. B; CHAPMAN, J. A et al.Cytogenetics and cell genetics. 1984, Vol 38, Num 4, pp 282-289, issn 0301-0171Article

Chromosomal localization of human and rat Aα, Bβ, and γ fibrinogen genes by in situ hybridizationMARINO, M. W; FULLER, G. M; ELDER, F. F. B et al.Cytogenetics and cell genetics. 1986, Vol 42, Num 1-2, pp 36-41, issn 0301-0171Article

Orthotopic ovarian transplantations in young and aged C57BL/6J micePARKENING, T. A; COLLINS, T. J; ELDER, F. F. B et al.Biology of reproduction. 1985, Vol 32, Num 5, pp 989-997, issn 0006-3363Article

Identical twins with deletion 16q syndrome: evidence that 16q12.2-q13 is the critical band regionELDER, F. F. B; FERGUSON, J. W; LOCKHART, L. H et al.Human genetics. 1984, Vol 67, Num 2, pp 233-236, issn 0340-6717Article

Cytogenetic abnormalities common to adenocarcinoma metastatic to the pleuraCAGLE, P. T; TAYLOR, L. D; SCHWARTZ, M. R et al.Cancer genetics and cytogenetics. 1989, Vol 39, Num 2, pp 219-225, issn 0165-4608Article

Neutropenia and defective chemotaxis associated with binuclear, tetraploid myeloid-monocytic leukocytesMAMLOK, R. J; JUNEJA, H. S; ELDER, F. F. B et al.The Journal of pediatrics. 1987, Vol 111, Num 4, pp 555-558, issn 0022-3476Article

Genomic DNA sequence, promoter expression, and chromosomal mapping of rat muscle carnitine palmitoyltransferase IDACHUN WANG; HARRISON, W; BUJA, L. M et al.Genomics (San Diego, Calif.). 1998, Vol 48, Num 3, pp 314-323, issn 0888-7543Article

Isodicentrix C chromosome in a patient with Turner syndrome - implications for localization of the X-inactivation centerPETTIGREW, A. L; MC CABE, E. R. B; ELDER, F. F. B et al.Human genetics. 1991, Vol 87, Num 4, pp 498-502, issn 0340-6717Article

Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4ALTHERR, M. R; BENGTSSON, U; ELDER, F. F. B et al.American journal of human genetics. 1991, Vol 49, Num 6, pp 1235-1242, issn 0002-9297Article

Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17GREENBERG, F; STRATTON, R. F; LOCKHART, L. H et al.American journal of medical genetics. 1986, Vol 23, Num 4, pp 853-859, issn 0148-7299Article

Insertional mutation of the collagen genes Col4a3 and Col4a4 in a mouse model of Alport syndromeWEI LU; PHILLIPS, C. L; KILLEN, P. D et al.Genomics (San Diego, Calif.). 1999, Vol 61, Num 2, pp 113-124, issn 0888-7543Article

Characterization of human DSPG3, a small dermatan sulfate proteoglycanDEERE, M; JOHNSON, J; GARZA, S et al.Genomics (San Diego, Calif.). 1996, Vol 38, Num 3, pp 399-404, issn 0888-7543Article

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosisSOHOCKI, M. M; BOWNE, S. J; HARRISON, W. R et al.Nature genetics. 2000, Vol 24, Num 1, pp 79-83, issn 1061-4036Article

A molecular cytogenetic analysis of X chromosome repatterning in the Bovidae : transpositions, inversions, and phylogenetic inferenceROBINSON, T. J; HARRISON, W. R; PONCE DE LEON, F. A et al.Cytogenetics and cell genetics. 1998, Vol 80, Num 1-4, pp 179-184, issn 0301-0171Article

Chromosome 1p36 deletions: The clinical phenotype and molecular characterization of a common newly delineated syndromeSHAPIRA, S. K; MCCASKILL, C; NORTHRUP, H et al.American journal of human genetics. 1997, Vol 61, Num 3, pp 642-650, issn 0002-9297Article

Chromosomes of Brants' whistling rat and genome conservation in the Otomyinae revealed by G-banding and fluorescence in situ hybridizationRAMBAU, R. V; HARRISON, W. R; ELDER, F. F. B et al.Cytogenetics and cell genetics. 1997, Vol 78, Num 3-4, pp 216-220, issn 0301-0171Conference Paper