Biesecker LG - Search Results

1

The end of the beginning of chromosome ends.

Biesecker LG. Biesecker LG. Am J Med Genet. 2002 Feb 1;107(4):263-6. doi: 10.1002/ajmg.10160. Am J Med Genet. 2002. PMID: 11840481 Review. No abstract available.

2

Severe anomalies associated with ring chromosome 7.

Biesecker LG, Cox B, Glover TW. Biesecker LG, et al. Am J Med Genet. 1991 Sep 15;40(4):429-31. doi: 10.1002/ajmg.1320400410. Am J Med Genet. 1991. PMID: 1746606

3

The Ohdo blepharophimosis syndrome: a third case.

Biesecker LG. Biesecker LG. J Med Genet. 1991 Feb;28(2):131-4. doi: 10.1136/jmg.28.2.131. J Med Genet. 1991. PMID: 2002485 Free PMC article.

4

Renal insufficiency in Williams syndrome.

Biesecker LG, Laxova R, Friedman A. Biesecker LG, et al. Am J Med Genet. 1987 Sep;28(1):131-5. doi: 10.1002/ajmg.1320280119. Am J Med Genet. 1987. PMID: 3314505 Review.

5

Case: responding to a request for genetic testing that is still in the lab.

Biesecker LG, Collins FS, DeRenzo EG, Grady C, MacKay CR. Biesecker LG, et al. Camb Q Healthc Ethics. 1995 Summer;4(3):387-400. Camb Q Healthc Ethics. 1995. PMID: 7551153 No abstract available.

6

Mild phenotypic manifestation of a 7p15.3p21.2 deletion.

Wang C, Maynard S, Glover TW, Biesecker LG. Wang C, et al. Among authors: biesecker lg. J Med Genet. 1993 Jul;30(7):610-2. doi: 10.1136/jmg.30.7.610. J Med Genet. 1993. PMID: 8411039 Free PMC article. Review.

7

Detection of a subtle rearrangement of chromosome 22 using molecular techniques.

Biesecker LG, Rosenberg M, Dziadzio L, Ledbetter DH, Ning Y, Sarneso C, Rosenbaum K. Biesecker LG, et al. Am J Med Genet. 1995 Sep 25;58(4):389-94. doi: 10.1002/ajmg.1320580426. Am J Med Genet. 1995. PMID: 8533859 Review.

8

Pfeiffer type cardiocranial syndrome: a third case report.

Williamson-Kruse L, Biesecker LG. Williamson-Kruse L, et al. Among authors: biesecker lg. J Med Genet. 1995 Nov;32(11):901-3. doi: 10.1136/jmg.32.11.901. J Med Genet. 1995. PMID: 8592338 Free PMC article. Review.

9

Isolation of the human chromosome 22q telomere and its application to detection of cryptic chromosomal abnormalities.

Ning Y, Rosenberg M, Biesecker LG, Ledbetter DH. Ning Y, et al. Among authors: biesecker lg. Hum Genet. 1996 Jun;97(6):765-9. doi: 10.1007/BF02346187. Hum Genet. 1996. PMID: 8641694

10

Characterization of familial partial 10p trisomy by chromosomal microdissection, FISH, and microsatellite dosage analysis.

Stone D, Ning Y, Guan XY, Kaiser-Kupfer M, Wynshaw-Boris A, Biesecker L. Stone D, et al. Hum Genet. 1996 Oct;98(4):396-402. doi: 10.1007/s004390050228. Hum Genet. 1996. PMID: 8792811

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