Stalker H - Search Results

1

A copy number variation morbidity map of developmental delay.

Cooper GM, Coe BP, Girirajan S, Rosenfeld JA, Vu TH, Baker C, Williams C, Stalker H, Hamid R, Hannig V, Abdel-Hamid H, Bader P, McCracken E, Niyazov D, Leppig K, Thiese H, Hummel M, Alexander N, Gorski J, Kussmann J, Shashi V, Johnson K, Rehder C, Ballif BC, Shaffer LG, Eichler EE. Cooper GM, et al. Among authors: stalker h. Nat Genet. 2011 Aug 14;43(9):838-46. doi: 10.1038/ng.909. Nat Genet. 2011. PMID: 21841781 Free PMC article.

2

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. 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

3

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.

4

Genotype-phenotype characterization in 13 individuals with chromosome Xp11.22 duplications.

Grams SE, Argiropoulos B, Lines M, Chakraborty P, Mcgowan-Jordan J, Geraghty MT, Tsang M, Eswara M, Tezcan K, Adams KL, Linck L, Himes P, Kostiner D, Zand DJ, Stalker H, Driscoll DJ, Huang T, Rosenfeld JA, Li X, Chen E. Grams SE, et al. Among authors: stalker h. Am J Med Genet A. 2016 Apr;170A(4):967-77. doi: 10.1002/ajmg.a.37519. Epub 2015 Dec 22. Am J Med Genet A. 2016. PMID: 26692240

5

Facial dysmorphism and digit anomalies in three siblings with severe developmental delay.

Mueller JM, Dagli AI, Stalker HJ, Rahman N, Zori RT, Williams CA. Mueller JM, et al. Clin Dysmorphol. 2011 Apr;20(2):92-94. doi: 10.1097/MCD.0b013e3283435174. Clin Dysmorphol. 2011. PMID: 21383553 No abstract available.

6

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.

7

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.

8

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. Among authors: stalker h. 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

9

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

10

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

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