Yen FF[Author] - Search Results

Year	Number of Results
1980	1
1981	1
1984	2
1985	1
1995	1
1997	1
1998	1
1999	1
2024	0

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

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

3

X chromatin and chromosome examination in aged women.

Yen FF, Matsuyama SS, Jarvik LF. Yen FF, et al. Mech Ageing Dev. 1981 May;16(1):55-60. doi: 10.1016/0047-6374(81)90031-2. Mech Ageing Dev. 1981. PMID: 7195966

4

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

5

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.

6

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

7

Vaginal uterine agenesis associated with amastia in a phenotypic female with a de novo 46,XX,t(8;13)(q22.1;q32.1) translocation.

Amesse L, Yen FF, Weisskopf B, Hertweck SP. Amesse L, et al. Among authors: yen ff. Clin Genet. 1999 Jun;55(6):493-5. doi: 10.1034/j.1399-0004.1999.550617.x. Clin Genet. 1999. PMID: 10450870 No abstract available.

8

A case of familial XY gonadal dysgenesis.

Hersh JH, Kable WT, Yen FF, Yussman MA, Weisskopf B. Hersh JH, et al. Among authors: yen ff. Fertil Steril. 1980 Dec;34(6):599-601. Fertil Steril. 1980. PMID: 7450079 Free article. No abstract available.

9

Gonadal and müllerian duct agenesis in a girl with 46,X,i(Xq).

De Leon FD, Hersh JH, Sanfilippo JS, Schikler KN, Yen FF. De Leon FD, et al. Among authors: yen ff. Obstet Gynecol. 1984 Mar;63(3 Suppl):81S-83S. Obstet Gynecol. 1984. PMID: 6700887

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