Papenhausen PR - Search Results

1

Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adult.

Papenhausen PR, Mueller OT, Johnson VP, Sutcliffe M, Diamond TM, Kousseff BG. Papenhausen PR, et al. Am J Med Genet. 1995 Nov 20;59(3):271-5. doi: 10.1002/ajmg.1320590302. Am J Med Genet. 1995. PMID: 8599348 Review.

2

Lowe oculocerebrorenal syndrome in a female with a balanced X;20 translocation: mapping of the X chromosome breakpoint.

Mueller OT, Hartsfield JK Jr, Gallardo LA, Essig YP, Miller KL, Papenhausen PR, Tedesco TA. Mueller OT, et al. Among authors: papenhausen pr. Am J Hum Genet. 1991 Oct;49(4):804-10. Am J Hum Genet. 1991. PMID: 1897526 Free PMC article.

3

Distinct 15q genotypes in Russell-Silver and ring 15 syndromes.

Rogan PK, Seip JR, Driscoll DJ, Papenhausen PR, Johnson VP, Raskin S, Woodward AL, Butler MG. Rogan PK, et al. Among authors: papenhausen pr. Am J Med Genet. 1996 Mar 1;62(1):10-5. doi: 10.1002/(SICI)1096-8628(19960301)62:1<10::AID-AJMG3>3.0.CO;2-#. Am J Med Genet. 1996. PMID: 8779316 Free PMC article.

4

Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adult.

Papenhausen PR, Mueller OT, Sutcliffe M, Diamond TM, Kousseff BG, Johnson VP. Papenhausen PR, et al. Am J Med Genet. 1996 Dec 2;66(1):90. doi: 10.1002/(SICI)1096-8628(19961202)66:1<90::AID-AJMG23>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8957521 No abstract available.

5

Cleft palate and complex chromosome rearrangements.

Kousseff BG, Papenhausen P, Neu RL, Essig YP, Saraceno CA. Kousseff BG, et al. Clin Genet. 1992 Sep;42(3):135-42. doi: 10.1111/j.1399-0004.1992.tb03225.x. Clin Genet. 1992. PMID: 1327590 Review.

6

Tissue limited mosaicism in a patient with tetrasomy 9p.

Papenhausen P, Riscile G, Miller K, Kousseff B, Tedesco T. Papenhausen P, et al. Am J Med Genet. 1990 Nov;37(3):388-91. doi: 10.1002/ajmg.1320370319. Am J Med Genet. 1990. PMID: 2260570

7

Complex chromosome rearrangement with ankyloblepharon filiforme adnatum.

Kousseff BG, Papenhausen P, Essig YP, Torres MP. Kousseff BG, et al. J Med Genet. 1993 Feb;30(2):167-70. doi: 10.1136/jmg.30.2.167. J Med Genet. 1993. PMID: 8445625 Free PMC article.

8

Cell line segregation in a 45,X/46,XY mosaic child with asymmetric leg growth.

Papenhausen PR, Mueller OT, Bercu B, Salazar J, Tedesco TA. Papenhausen PR, et al. Clin Genet. 1991 Sep;40(3):237-41. doi: 10.1111/j.1399-0004.1991.tb03084.x. Clin Genet. 1991. PMID: 1773540

9

Twin-twin transfusion syndrome in a dizygotic monochorionic-diamniotic twin pregnancy.

Quintero RA, Mueller OT, Martínez JM, Arroyo J, Gilbert-Barness E, Hilbelink D, Papenhausen P, Sutcliffe M. Quintero RA, et al. J Matern Fetal Neonatal Med. 2003 Oct;14(4):279-81. doi: 10.1080/jmf.14.4.279.281. J Matern Fetal Neonatal Med. 2003. PMID: 14738176

10

Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocation.

Joseph M, Cantú ES, Pai GS, Willi SM, Papenhausen PR, Weiss L. Joseph M, et al. Among authors: papenhausen pr. J Med Genet. 1996 Nov;33(11):906-11. doi: 10.1136/jmg.33.11.906. J Med Genet. 1996. PMID: 8950669 Free PMC article.

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