Mowrey PN - Search Results

1

Neurologic manifestations in 18q- syndrome.

Miller G, Mowrey PN, Hopper KD, Frankel CA, Ladda RL. Miller G, et al. Among authors: mowrey pn. Am J Med Genet. 1990 Sep;37(1):128-32. doi: 10.1002/ajmg.1320370130. Am J Med Genet. 1990. PMID: 1700607

2

Malformations in a child with dup (7pter-p15.1) and del (7q36-qter) as a result of familial pericentric inversion.

Ramer JC, Mowrey PN, Ladda RL. Ramer JC, et al. Among authors: mowrey pn. Clin Genet. 1991 Jun;39(6):442-50. doi: 10.1111/j.1399-0004.1991.tb03056.x. Clin Genet. 1991. PMID: 1863992

3

Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: review of brain, cardiac, and limb malformations.

Ramer JC, Mowrey PN, Robins DB, Ligato S, Towfighi J, Ladda RL. Ramer JC, et al. Among authors: mowrey pn. Am J Med Genet. 1990 Nov;37(3):392-400. doi: 10.1002/ajmg.1320370320. Am J Med Genet. 1990. PMID: 2260571 Review.

4

Clinical and molecular analyses of deletion 3p25-pter syndrome.

Mowrey PN, Chorney MJ, Venditti CP, Latif F, Modi WS, Lerman MI, Zbar B, Robins DB, Rogan PK, Ladda RL. Mowrey PN, et al. Am J Med Genet. 1993 Jul 1;46(6):623-9. doi: 10.1002/ajmg.1320460604. Am J Med Genet. 1993. PMID: 8103286

5

46,XX, inv(6)(p21.1p23) in a pedigree with hereditary haemochromatosis.

Venditti CP, Seese NK, Gerhard GS, Ten Elshof AE, Chorney KA, Mowrey PN, Lacey PG, Knoll JH, Chorney MJ. Venditti CP, et al. Among authors: mowrey pn. J Med Genet. 1997 Jan;34(1):24-7. doi: 10.1136/jmg.34.1.24. J Med Genet. 1997. PMID: 9032645 Free PMC article.

6

Molecularly defined interstitial tandem duplication 6p case with mild manifestations.

Ng D, Mowrey P, Ragoussis J, Mirza G, Coll E, Di Fazio MP, Turner C, Levin SW. Ng D, et al. Am J Med Genet. 2001 Nov 1;103(4):320-5. Am J Med Genet. 2001. PMID: 11746013

7

Interstitial del(13q) associated with blindness and mental retardation.

Juberg RC, Mowrey PN. Juberg RC, et al. Among authors: mowrey pn. Am J Med Genet. 1984 Mar;17(3):609-13. doi: 10.1002/ajmg.1320170309. Am J Med Genet. 1984. PMID: 6711612

8

Unexpected retention and concomitant loss of subtelomeric regions in balanced chromosome anomalies by FISH.

Pettenati MJ, Jackle B, Bobby P, Stewart W, Von Kap-Herr C, Mowrey P, Rao PN, May KM. Pettenati MJ, et al. Among authors: mowrey p. Am J Med Genet. 2002 Jul 22;111(1):48-53. doi: 10.1002/ajmg.10535. Am J Med Genet. 2002. PMID: 12124733

9

Should the 3C (craniocerebellocardiac) syndrome be included in the spectrum of velocardiofacial syndrome and DiGeorge sequence?

Butler MG, Mowrey P. Butler MG, et al. J Med Genet. 1996 Aug;33(8):719-20. doi: 10.1136/jmg.33.8.719-a. J Med Genet. 1996. PMID: 8863172 Free PMC article. No abstract available.

10

Origin of nondisjunction in trisomy 21 syndrome: all studies compiled, parental age analysis, and international comparisons.

Juberg RC, Mowrey PN. Juberg RC, et al. Among authors: mowrey pn. Am J Med Genet. 1983 Sep;16(1):111-6. doi: 10.1002/ajmg.1320160117. Am J Med Genet. 1983. PMID: 6227238

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