Korf BR - Search Results

1

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

2

Galactose metabolism and reproductive history in women with type 1 neurofibromatosis.

Cramer DW, Korf BR, Fortier LJ. Cramer DW, et al. Among authors: korf br. Am J Med Genet. 1991 Jun 15;39(4):502-8. doi: 10.1002/ajmg.1320390432. Am J Med Genet. 1991. PMID: 1908637

3

Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1).

Seizinger BR, Farmer GE, Haines JL, Ozelius LJ, Anderson K, Korf BR, Parry DM, Pericak-Vance MA, Mulvihill JJ, Menon A, et al. Seizinger BR, et al. Among authors: korf br. Am J Hum Genet. 1989 Jan;44(1):30-2. Am J Hum Genet. 1989. PMID: 2491778 Free PMC article.

4

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

5

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

6

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

7

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

8

Limb anomalies in DiGeorge and CHARGE syndromes.

Prasad C, Quackenbush EJ, Whiteman D, Korf B. Prasad C, et al. 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

9

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

10

Complex familial rearrangement of chromosome 9p24.3 detected by FISH.

Repetto GM, Wagstaff J, Korf BR, Knoll JH. Repetto GM, et al. Among authors: korf br. Am J Med Genet. 1998 Apr 1;76(4):306-9. Am J Med Genet. 1998. PMID: 9545094

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