Wyandt HE - Search Results

1

Summary of the 1993 ASHG ancillary meeting "recent research on chromosome 4p syndromes and genes".

Estabrooks LL, Breg WR, Hayden MR, Ledbetter DH, Myers RM, Wyandt HE, Yang-Feng TL, Hirschhorn K. Estabrooks LL, et al. Among authors: wyandt he. Am J Med Genet. 1995 Feb 13;55(4):453-8. doi: 10.1002/ajmg.1320550412. Am J Med Genet. 1995. PMID: 7762585 Review.

2

Characterization of a duplication in the terminal band of 4p by molecular cytogenetics.

Wyandt HE, Milunsky J, Lerner T, Gusella JF, Hou A, MacDonald M, Adekunle S, Milunsky A. Wyandt HE, et al. Am J Med Genet. 1993 Apr 1;46(1):72-6. doi: 10.1002/ajmg.1320460112. Am J Med Genet. 1993. PMID: 7684190

3

The Interregional Cytogenetic Register System (ICRS).

Prescott GH, Rivas ML, Shanbeck L, Macfarlane DW, Wyandt HE, Breg WR, Lubs HA, Magenis RE, Summitt RL, Palmer CG, Hecht F, Kimberling W, Clow D. Prescott GH, et al. Among authors: wyandt he. Birth Defects Orig Artic Ser. 1978;14(6C):269-79. Birth Defects Orig Artic Ser. 1978. PMID: 310323 No abstract available.

4

Tandem duplication/deletion in a maternally derived chromosome 9 supernumerary derivative resulting in 9p trisomy and partial 9q tetrasomy.

Wyandt HE, Lebo RV, Fenerci EY, Sadhu DN, Milunsky JM. Wyandt HE, et al. Am J Med Genet. 2000 Aug 14;93(4):305-12. Am J Med Genet. 2000. PMID: 10946358

5

Transmission of ring 14 chromosome from mother to two sons.

Matalon R, Supple P, Wyandt H, Rosenthal IM. Matalon R, et al. Am J Med Genet. 1990 Aug;36(4):381-5. doi: 10.1002/ajmg.1320360402. Am J Med Genet. 1990. PMID: 2202211 Review.

6

Chromosome deletion of Xq25 in an individual with X-linked lymphoproliferative disease.

Wyandt HE, Grierson HL, Sanger WG, Skare JC, Milunsky A, Purtilo DT. Wyandt HE, et al. Am J Med Genet. 1989 Jul;33(3):426-30. doi: 10.1002/ajmg.1320330331. Am J Med Genet. 1989. PMID: 2801783

7

Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24).

Haddad BR, Lin AE, Wyandt H, Milunsky A. Haddad BR, et al. J Med Genet. 1996 Dec;33(12):1045-7. doi: 10.1136/jmg.33.12.1045. J Med Genet. 1996. PMID: 9004142 Free PMC article.

8

Partial duplication of Xp: a case report and review of previously reported cases.

Wyandt HE, Bugeau-Michaud L, Skare JC, Milunsky A. Wyandt HE, et al. Am J Med Genet. 1991 Sep 1;40(3):280-3. doi: 10.1002/ajmg.1320400306. Am J Med Genet. 1991. PMID: 1951429 Review.

9

De novo 21q interstitial deletion in a retarded boy with ulno-fibular dysostosis.

Reynolds JF, Wyandt HE, Kelly TE. Reynolds JF, et al. Among authors: wyandt he. Am J Med Genet. 1985 Jan;20(1):173-80. doi: 10.1002/ajmg.1320200121. Am J Med Genet. 1985. PMID: 3970070

10

Trisomy 4p in four relatives: variability and lack of distinctive features in phenotypic expression.

Reynolds JF, Shires MA, Wyandt HE, Kelly TE. Reynolds JF, et al. Among authors: wyandt he. Clin Genet. 1983 Nov;24(5):365-74. doi: 10.1111/j.1399-0004.1983.tb00087.x. Clin Genet. 1983. PMID: 6418421

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

90 results

Search Page

Filters