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Items: 11

1.

Rapid detection of chromosome aneuploidies by prenatal interphase FISH (fluorescence in situ hybridization) and its clinical utility in Japan.

Sawa R, Hayashi Z, Tanaka T, Onda T, Hoshi K, Fukada Y, Takai Y, Taketani Y, Kubo T, Hamada H, Yoshida K, Nakamura Y, Okai T, Sakai M, Kaneoka T, Makino Y, Aono T, Maeda K, Honda R, Okamura H, Sago H, Kitagawa M, Minoura S, Inaba J, Terakawa N, Nagata N, Shimomura K, Sapeta MJ, Estabrooks LL.

J Obstet Gynaecol Res. 2001 Feb;27(1):41-7.

PMID:
11330730
2.
3.

Antibody deficiency in Wolf-Hirschhorn syndrome.

Hanley-Lopez J, Estabrooks LL, Stiehm R.

J Pediatr. 1998 Jul;133(1):141-3.

PMID:
9672528
4.

Albright hereditary osteodystrophy and del(2) (q37.3) in four unrelated individuals.

Phelan MC, Rogers RC, Clarkson KB, Bowyer FP, Levine MA, Estabrooks LL, Severson MC, Dobyns WB.

Am J Med Genet. 1995 Jul 31;58(1):1-7.

PMID:
7573148
5.

Preliminary phenotypic map of chromosome 4p16 based on 4p deletions.

Estabrooks LL, Rao KW, Driscoll DA, Crandall BF, Dean JC, Ikonen E, Korf B, Aylsworth AS.

Am J Med Genet. 1995 Jul 17;57(4):581-6.

PMID:
7573133
6.

Summary of the 1993 ASHG ancillary meeting "recent research on chromosome 4p syndromes and genes".

Estabrooks LL, Breg WR, Hayden MR, Ledbetter DH, Myers RM, Wyandt HE, Yang-Feng TL, Hirschhorn K.

Am J Med Genet. 1995 Feb 13;55(4):453-8. Review.

PMID:
7762585
7.

Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome.

Estabrooks LL, Lamb AN, Aylsworth AS, Callanan NP, Rao KW.

J Med Genet. 1994 Feb;31(2):103-7.

8.

Interstitial deletion of distal chromosome 4p in a patient without classical Wolf-Hirschhorn syndrome.

Estabrooks LL, Rao KW, Korf B.

Am J Med Genet. 1993 Jan 1;45(1):97-100.

PMID:
8418669
9.
10.

Inhibition of replicon initiation in human cells following stabilization of topoisomerase-DNA cleavable complexes.

Kaufmann WK, Boyer JC, Estabrooks LL, Wilson SJ.

Mol Cell Biol. 1991 Jul;11(7):3711-8.

11.

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

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