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Items: 1 to 20 of 26

1.

Physical mapping of the holoprosencephaly critical region on chromosome 7q36.

Gurrieri F, Trask BJ, van den Engh G, Krauss CM, Schinzel A, Pettenati MJ, Schindler D, Dietz-Band J, Vergnaud G, Scherer SW, et al.

Nat Genet. 1993 Mar;3(3):247-51.

PMID:
8485580
2.

Report of the Fourth International Workshop on Human Chromosome 21.

Delabar JM, Créau N, Sinet PM, Ritter O, Antonarakis SE, Burmeister M, Chakravarti A, Nizetic D, Ohki M, Patterson D, et al.

Genomics. 1993 Dec;18(3):735-45. No abstract available.

PMID:
8307590
3.

Down syndrome phenotypes: the consequences of chromosomal imbalance.

Korenberg JR, Chen XN, Schipper R, Sun Z, Gonsky R, Gerwehr S, Carpenter N, Daumer C, Dignan P, Disteche C, et al.

Proc Natl Acad Sci U S A. 1994 May 24;91(11):4997-5001.

4.

Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity.

Muenke M, Gurrieri F, Bay C, Yi DH, Collins AL, Johnson VP, Hennekam RC, Schaefer GB, Weik L, Lubinsky MS, et al.

Proc Natl Acad Sci U S A. 1994 Aug 16;91(17):8102-6.

5.

Localization of the squalene synthase gene (FDFT1) to human chromosome 8p22-p23.1.

Schechter I, Conrad DG, Hart I, Berger RC, McKenzie TL, Bleskan J, Patterson D.

Genomics. 1994 Mar 1;20(1):116-8.

PMID:
8020937
6.

A transcript map of the Down syndrome critical region on chromosome 21.

Peterson A, Patil N, Robbins C, Wang L, Cox DR, Myers RM.

Hum Mol Genet. 1994 Oct;3(10):1735-42.

PMID:
7849696
7.

Positional cloning moves from perditional to traditional.

Collins FS.

Nat Genet. 1995 Apr;9(4):347-50. Erratum in: Nat Genet 1995 Sep;11(1):104.

PMID:
7795639
8.

Report and abstracts of the Fifth International Workshop on Human Chromosome 21 Mapping 1994. Tsukuba, Japan, November 9-11, 1994.

[No authors listed]

Cytogenet Cell Genet. 1995;70(3-4):147-82. No abstract available.

PMID:
7789165
9.

Physical mapping of the holoprosencephaly critical region in 18p11.3.

Overhauser J, Mitchell HF, Zackai EH, Tick DB, Rojas K, Muenke M.

Am J Hum Genet. 1995 Nov;57(5):1080-5.

10.

A male infant with holoprosencephaly, associated with ring chromosome 21.

Aronson DC, Jansweijer MC, Hoovers JM, Barth PG.

Clin Genet. 1987 Jan;31(1):48-52.

PMID:
3568433
11.
12.

Partial physical map of human chromosome 21.

Gardiner K, Watkins P, Münke M, Drabkin H, Jones C, Patterson D.

Somat Cell Mol Genet. 1988 Nov;14(6):623-37.

PMID:
3194801
13.

Irradiation-reduced human chromosome 21 hybrids.

Graw S, Davidson J, Gusella J, Watkins P, Tanzi R, Neve R, Patterson D.

Somat Cell Mol Genet. 1988 May;14(3):233-42.

PMID:
3163426
14.

Regional localization of DNA sequences on chromosome 21 using somatic cell hybrids.

Van Keuren ML, Watkins PC, Drabkin HA, Jabs EW, Gusella JF, Patterson D.

Am J Hum Genet. 1986 Jun;38(6):793-804.

15.

Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology.

Cohen MM Jr.

Teratology. 1989 Sep;40(3):211-35. Review.

PMID:
2688166
16.

Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly.

Münke M.

Am J Med Genet. 1989 Oct;34(2):237-45. Review. No abstract available.

PMID:
2683787
17.

A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids.

Glaser T, Housman D, Lewis WH, Gerhard D, Jones C.

Somat Cell Mol Genet. 1989 Nov;15(6):477-501.

PMID:
2595451
18.

Holoprosencephaly in an infant with a minute deletion of chromosome 21(q22.3).

Estabrooks LL, Rao KW, Donahue RP, Aylsworth AS.

Am J Med Genet. 1990 Jul;36(3):306-9.

PMID:
2363428
19.
20.

Sublocalization on chromosome 21 of human interferon-alpha receptor gene and the gene for an interferon-gamma response protein.

Langer JA, Rashidbaigi A, Lai LW, Patterson D, Jones C.

Somat Cell Mol Genet. 1990 May;16(3):231-40.

PMID:
2141727
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