Stalker HJ - Search Results

1

Genetic counseling in Angelman syndrome: gonadal mosaicism.

Stalker HJ, Williams CA, Wagstaff J. Stalker HJ, et al. Am J Med Genet. 1998 Aug 6;78(5):482. Am J Med Genet. 1998. PMID: 9714017 No abstract available.

2

Genetic counseling in Angelman syndrome: the challenges of multiple causes.

Stalker HJ, Williams CA. Stalker HJ, et al. Am J Med Genet. 1998 Apr 28;77(1):54-9. Am J Med Genet. 1998. PMID: 9557895 Review.

3

Angelman syndrome.

Williams CA, Zori RT, Hendrickson J, Stalker H, Marum T, Whidden E, Driscoll DJ. Williams CA, et al. Curr Probl Pediatr. 1995 Aug;25(7):216-31. doi: 10.1016/s0045-9380(06)80036-8. Curr Probl Pediatr. 1995. PMID: 8521718 Review. No abstract available.

4

Concurrence of supravalvular aortic stenosis and peripheral pulmonary stenosis in three generations of a family: a form of arterial dysplasia.

Kumar A, Stalker HJ, Williams CA. Kumar A, et al. Among authors: stalker hj. Am J Med Genet. 1993 Mar 15;45(6):739-42. doi: 10.1002/ajmg.1320450614. Am J Med Genet. 1993. PMID: 8456853 Review.

5

Juvenile rheumatoid arthritis in velo-cardio-facial syndrome: coincidence or unusual complication?

Rasmussen SA, Williams CA, Ayoub EM, Sleasman JW, Gray BA, Bent-Williams A, Stalker HJ, Zori RT. Rasmussen SA, et al. Among authors: stalker hj. Am J Med Genet. 1996 Sep 6;64(4):546-50. doi: 10.1002/(SICI)1096-8628(19960906)64:4<546::AID-AJMG4>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8870920

6

Prevalence of 22q11 region deletions in patients with velopharyngeal insufficiency.

Zori RT, Boyar FZ, Williams WN, Gray BA, Bent-Williams A, Stalker HJ, Rimer LA, Nackashi JA, Driscoll DJ, Rasmussen SA, Dixon-Wood V, Williams CA. Zori RT, et al. Among authors: stalker hj. Am J Med Genet. 1998 Apr 28;77(1):8-11. Am J Med Genet. 1998. PMID: 9557885

7

A patient with the syndrome of megalencephaly, mega corpus callosum and complete lack of motor development.

Dagli AI, Stalker HJ, Williams CA. Dagli AI, et al. Among authors: stalker hj. Am J Med Genet A. 2008 Jan 15;146A(2):204-7. doi: 10.1002/ajmg.a.32079. Am J Med Genet A. 2008. PMID: 18076119

8

A family with a grand-maternally derived interstitial duplication of proximal 15q.

Boyar FZ, Whitney MM, Lossie AC, Gray BA, Keller KL, Stalker HJ, Zori RT, Geffken G, Mutch J, Edge PJ, Voeller KS, Williams CA, Driscoll DJ. Boyar FZ, et al. Among authors: stalker hj. Clin Genet. 2001 Dec;60(6):421-30. doi: 10.1034/j.1399-0004.2001.600604.x. Clin Genet. 2001. PMID: 11846734

9

Routine cytogenetic and FISH studies for 17p11/15q11 duplications and subtelomeric rearrangement studies in children with autism spectrum disorders.

Keller K, Williams C, Wharton P, Paulk M, Bent-Williams A, Gray B, Ward A, Stalker H, Wallace M, Carter R, Zori R. Keller K, et al. Am J Med Genet A. 2003 Mar 1;117A(2):105-11. doi: 10.1002/ajmg.a.10042. Am J Med Genet A. 2003. PMID: 12567405

10

Analysis of CpG C-to-T mutations in neurofibromatosis type 1. Mutations in brief no. 129. Online.

Krkljus S, Abernathy CR, Johnson JS, Williams CA, Driscoll DJ, Zori R, Stalker HJ, Rasmussen SA, Collins FS, Kousseff BG, Baumbach L, Wallace MR. Krkljus S, et al. Among authors: stalker hj. Hum Mutat. 1998;11(5):411. doi: 10.1002/(SICI)1098-1004(1998)11:5<411::AID-HUMU11>3.0.CO;2-2. Hum Mutat. 1998. PMID: 10336779

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