Yen FF - Search Results

1

Changing phenotype in Floating-Harbor syndrome.

Hersh JH, Groom KR, Yen FF, Verdi GD. Hersh JH, et al. Among authors: yen ff. Am J Med Genet. 1998 Feb 26;76(1):58-61. Am J Med Genet. 1998. PMID: 9508066 Review.

2

Patient with terminal duplication 3q and terminal deletion 5q: comparison with the 3q duplication syndrome and distal 5q deletion syndrome.

Angle B, Yen F, Hersh JH, Gowans G. Angle B, et al. Am J Med Genet A. 2003 Feb 1;116A(4):376-80. doi: 10.1002/ajmg.a.10025. Am J Med Genet A. 2003. PMID: 12522795

3

Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality.

Williams PG, Hersh JH, Yen FF, Barch MJ, Kleinert HE, Kunz J, Kalff-Suske M. Williams PG, et al. Among authors: yen ff. Clin Genet. 1997 Dec;52(6):436-41. doi: 10.1111/j.1399-0004.1997.tb02565.x. Clin Genet. 1997. PMID: 9520255

4

XY gonadal dysgenesis associated with a multiple pterygium syndrome phenotype.

Angle B, Hersh JH, Yen F, Verdi GD. Angle B, et al. Am J Med Genet. 1997 Jan 10;68(1):7-11. Am J Med Genet. 1997. PMID: 8986268

5

Case of partial duplication 2q3 with characteristic phenotype: rare occurrence of an unbalanced offspring resulting from a parental pericentric inversion.

Angle B, Hersh JH, Yen F, Christensen KM. Angle B, et al. Am J Med Genet. 2000 Mar 13;91(2):126-30. doi: 10.1002/(sici)1096-8628(20000313)91:2<126::aid-ajmg9>3.0.co;2-h. Am J Med Genet. 2000. PMID: 10748411

6

Partial duplication 4q and deletion 1p36 in monozygotic twins with discordant phenotypes.

Angle B, Yen F, Hersh JH, Gowans G, Barch M. Angle B, et al. Am J Med Genet. 2002 Aug 15;111(3):307-12. doi: 10.1002/ajmg.10599. Am J Med Genet. 2002. PMID: 12210328

7

De novo 1;10 balanced translocation in an infant with thanatophoric dysplasia: a clue to the locus of the candidate gene.

Hersh JH, Yen FF, Peiper SC, Barch MJ, Yacoub OA, Voss DH, Roberts JL. Hersh JH, et al. Among authors: yen ff. J Med Genet. 1995 Apr;32(4):293-5. doi: 10.1136/jmg.32.4.293. J Med Genet. 1995. PMID: 7643360 Free PMC article.

8

Mild intellectual deficits in a child with 49,XXXXY.

Hersh JH, Bloom AS, Yen F, Topinka C, Weisskopf B. Hersh JH, et al. Res Dev Disabil. 1988;9(2):171-6. doi: 10.1016/0891-4222(88)90050-9. Res Dev Disabil. 1988. PMID: 3406471

9

Tetraploidy: a report of three live-born infants.

Scarbrough PR, Hersh J, Kukolich MK, Carroll AJ, Finley SC, Hochberger R, Wilkerson S, Yen FF, Althaus BW. Scarbrough PR, et al. Among authors: yen ff. Am J Med Genet. 1984 Sep;19(1):29-37. doi: 10.1002/ajmg.1320190106. Am J Med Genet. 1984. PMID: 6496571

10

Dup(4p)del(9p) in a familial mental retardation syndrome. Resemblance to de Lange syndrome detected by high-resolution banding.

Hersh JH, Dale KS, Gerald PS, Yen FF, Weisskopf B, Dinno ND. Hersh JH, et al. Among authors: yen ff. Am J Dis Child. 1985 Jan;139(1):81-4. doi: 10.1001/archpedi.1985.02140030087037. Am J Dis Child. 1985. PMID: 3969990

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