Minireview : cryptic translocations and telomere integrityLEDBETTER, D. H.American journal of human genetics. 1992, Vol 51, Num 3, pp 451-456, issn 0002-9297Article

The colorizing' of cytogenetics: is it ready for prime time?LEDBETTER, D. H.Human molecular genetics (Print). 1992, Vol 1, Num 5, pp 297-299, issn 0964-6906Article

Dinucleotide repeat polymorphism mapping to the critical region for lissencephaly (17p13.3)CARROZZO, R; LEDBETTER, D. H.Human molecular genetics (Print). 1993, Vol 2, Num 5, issn 0964-6906, p. 615Article

Uniparental disomy in humans : development of an imprinting map and its implications for prenatal diagnosisLEDBETTER, D. H; ENGEL, E.Human molecular genetics (Print). 1995, Vol 4, pp 1757-1764, issn 0964-6906, REVIEWArticle

Report of the committee on the constitution of chromosome 17SOLOMON, E; LEDBETTER, D. H.Cytogenetics and cell genetics. 1990, Vol 55, Num 1-4, pp 198-215, issn 0301-0171, 18 p.Conference Paper

Molecular cloning and characterization of the human NUDC geneMATSUMOTO, N; LEDBETTER, D. H.Human genetics. 1999, Vol 104, Num 6, pp 498-504, issn 0340-6717Article

Genomic structure, chromosomal mapping, and expression pattern of human DCAMKL1 (KIAA0369), a homologue of DCX (XLIS)MATSUMOTO, N; PILZ, D. T; LEDBETTER, D. H et al.Genomics (San Diego, Calif.). 1999, Vol 56, Num 2, pp 179-183, issn 0888-7543Article

Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to a terminal del(22q)HERMAN, G. E; GREENBERG, F; LEDBETTER, D. H et al.American journal of medical genetics. 1988, Vol 29, Num 4, pp 909-915, issn 0148-7299Article

Fragile X syndrome: a unique mutation in manNUSSBAUM, R. L; LEDBETTER, D. H.Annual review of genetics. 1986, Vol 20, pp 109-145, issn 0066-4197Article

A common fragile site at Xq27: theoretical and practical implicationsLEDBETTER, S. A; LEDBETTER, D. H.American journal of human genetics. 1988, Vol 42, Num 5, pp 694-702, issn 0002-9297Article

Lissencephaly : a human brain maformation associated with deletion of the LIS1 gene located at chromosome 17p13DOBYNS, W. B; CARROZZO, R; LEDBETTER, D. H et al.JAMA, the journal of the American Medical Association. 1993, Vol 270, Num 23, pp 2838-2842, issn 0098-7484Article

Interstitial deletion of chromosome 18[del(18)q11.2q12.2 or q12.2q21.1]SURH, L. C; LEDBETTER, D. H; GREENBERG, F et al.American journal of medical genetics. 1991, Vol 41, Num 1, pp 15-17, issn 0148-7299Article

Fra(10)(q25): the BrdU effect is substitution-dependentGOLLIN, S. M; HOLMQUIST, G. P; LEDBETTER, D. H et al.American journal of human genetics. 1985, Vol 37, Num 1, pp 208-214, issn 0002-9297Article

Classical lissencephaly syndromes : does the face reflect the brain?ALLANSON, J. E; LEDBETTER, D. H; DOBYNS, W. B et al.Journal of medical genetics. 1998, Vol 35, Num 11, pp 920-923, issn 0022-2593Article

Determination of the origin of nondisjunction in a49,XXXXX male using hypervariable dinucleotide repeat sequencesHUANG, T. H.-M; GREENBERG, F; LEDBETTER, D. H et al.Human genetics. 1991, Vol 86, Num 6, pp 619-620, issn 0340-6717Article

Chromosomal assignment and regional localization of myeloperoxidase in the mouseROBINSON, T. J; MORRIS, D. J; LEDBETTER, D. H et al.Cytogenetics and cell genetics. 1990, Vol 53, Num 2-3, pp 83-86, issn 0301-0171Article

New X-linked mental retardation disorder with Dandy-Walker malformation, basal ganglia disease and seizuresPETTIGREW, A. L; JACKSON, L. G; LEDBETTER, D. H et al.American journal of medical genetics. 1991, Vol 38, Num 2-3, pp 200-207, issn 0148-7299Article

Implications of fragile X expression in normal males for the nature of the mutationLEDBETTER, D. H; LEDBETTER, S. A; NUSSBAUM, R. L et al.Nature (London). 1986, Vol 324, Num 6093, pp 161-163, issn 0028-0836Article

Isolation of the human chromosome 22q telomere and its application to detection of cryptic chromosomal abnormalitiesNING, Y; ROSENBERG, M; BIESECKER, L. G et al.Human genetics. 1996, Vol 97, Num 6, pp 765-769, issn 0340-6717Article

Expression of the fragile (X) chromosome in an interspecific somatic cell hybridNUSSBAUM, R. L; AIRHART, S. D; LEDBETTER, D. H et al.Human genetics. 1983, Vol 64, Num 2, pp 148-150, issn 0340-6717Article

Significance of genetic testing for paternal uniparental disomy of chromosome 6 in neonatal mellitusCHRISTIAN, S. L; RICH, B. H; LOEBL, C et al.The Journal of pediatrics. 1999, Vol 134, Num 1, pp 42-46, issn 0022-3476Article

Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1PILZ, D. T; KUC, J; MATSUMOTO, N et al.Human molecular genetics (Print). 1999, Vol 8, Num 9, pp 1757-1760, issn 0964-6906Article

Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethalityHIROTSUNE, S; FLECK, M. W; GAMBELLO, M. J et al.Nature genetics. 1998, Vol 19, Num 4, pp 333-339, issn 1061-4036Article

Molecular screening for proximal 15q abnormalities in a mentally retarded populationJACOBSEN, J; KING, B. H; LEVENTHAL, B. L et al.Journal of medical genetics. 1998, Vol 35, Num 7, pp 534-538, issn 0022-2593Article

Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS) : a gene causing neuronal migration defects in human brainROSS, M. E; ALLEN, K. M; CZAPANSKY-BIELMAN, D et al.Human molecular genetics (Print). 1997, Vol 6, Num 4, pp 555-562, issn 0964-6906Article