Korf B - Search Results

1

Limb anomalies in DiGeorge and CHARGE syndromes.

Prasad C, Quackenbush EJ, Whiteman D, Korf B. Prasad C, et al. Among authors: korf b. Am J Med Genet. 1997 Jan 20;68(2):179-81. doi: 10.1002/(sici)1096-8628(19970120)68:2<179::aid-ajmg11>3.0.co;2-r. Am J Med Genet. 1997. PMID: 9028454

2

17q inversion involving the neurofibromatosis type one locus in a family with neurofibromatosis type one.

Asamoah A, North K, Doran S, Wagstaff J, Ogle R, Collins FS, Korf BR. Asamoah A, et al. Among authors: korf br. Am J Med Genet. 1995 Aug 14;60(4):312-6. doi: 10.1002/ajmg.1320600410. Am J Med Genet. 1995. PMID: 7485267

3

CHARGE association in a child with de novo inverted duplication (14)(q22-->q24.3).

North KN, Wu BL, Cao BN, Whiteman DA, Korf BR. North KN, et al. Among authors: korf br. Am J Med Genet. 1995 Jul 17;57(4):610-4. doi: 10.1002/ajmg.1320570419. Am J Med Genet. 1995. PMID: 7573139

4

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

Estabrooks LL, Rao KW, Korf B. Estabrooks LL, et al. Among authors: korf b. Am J Med Genet. 1993 Jan 1;45(1):97-100. doi: 10.1002/ajmg.1320450123. Am J Med Genet. 1993. PMID: 8418669

5

Deletion of the entire NF1 gene detected by the FISH: four deletion patients associated with severe manifestations.

Wu BL, Austin MA, Schneider GH, Boles RG, Korf BR. Wu BL, et al. Among authors: korf br. Am J Med Genet. 1995 Dec 4;59(4):528-35. doi: 10.1002/ajmg.1320590427. Am J Med Genet. 1995. PMID: 8585580

6

Neurobehavioral profiles of children with neurofibromatosis 1 referred for learning disabilities are sex-specific.

Chapman CA, Waber DP, Bassett N, Urion DK, Korf BR. Chapman CA, et al. Among authors: korf br. Am J Med Genet. 1996 Apr 9;67(2):127-32. doi: 10.1002/(SICI)1096-8628(19960409)67:2<127::AID-AJMG1>3.0.CO;2-P. Am J Med Genet. 1996. PMID: 8723038

7

Allele-specific replication of 15q11-q13 loci: a diagnostic test for detection of uniparental disomy.

White LM, Rogan PK, Nicholls RD, Wu BL, Korf B, Knoll JH. White LM, et al. Among authors: korf b. Am J Hum Genet. 1996 Aug;59(2):423-30. Am J Hum Genet. 1996. PMID: 8755930 Free PMC article.

8

Distal 8p deletion (8)(p23.1): an easily missed chromosomal abnormality that may be associated with congenital heart defect and mental retardation.

Wu BL, Schneider GH, Sabatino DE, Bozovic LZ, Cao B, Korf BR. Wu BL, et al. Among authors: korf br. Am J Med Genet. 1996 Mar 1;62(1):77-83. doi: 10.1002/(SICI)1096-8628(19960301)62:1<77::AID-AJMG16>3.0.CO;2-S. Am J Med Genet. 1996. PMID: 8779331

9

Somatic mosaicism for deletion of the entire NF1 gene identified by FISH.

Wu BL, Boles RG, Yaari H, Weremowicz S, Schneider GH, Korf BR. Wu BL, et al. Among authors: korf br. Hum Genet. 1997 Feb;99(2):209-13. doi: 10.1007/s004390050341. Hum Genet. 1997. PMID: 9048923

10

Deletion of the entire NF1 gene causing distinct manifestations in a family.

Wu BL, Schneider GH, Korf BR. Wu BL, et al. Among authors: korf br. Am J Med Genet. 1997 Mar 3;69(1):98-101. Am J Med Genet. 1997. PMID: 9066892

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

318 results

Search Page

Filters