Hopkin RJ - Search Results

1

Fractures in children with neurofibromatosis type 1 from two NF clinics.

George-Abraham JK, Martin LJ, Kalkwarf HJ, Rieley MB, Stevenson DA, Viskochil DH, Hopkin RJ, Stevens AM, Hanson H, Schorry EK. George-Abraham JK, et al. Among authors: hopkin rj. Am J Med Genet A. 2013 May;161A(5):921-6. doi: 10.1002/ajmg.a.35541. Epub 2013 Mar 25. Am J Med Genet A. 2013. PMID: 23529831

2

New insights into the phenotypes of 6q deletions.

Hopkin RJ, Schorry E, Bofinger M, Milatovich A, Stern HJ, Jayne C, Saal HM. Hopkin RJ, et al. Am J Med Genet. 1997 Jun 27;70(4):377-86. Am J Med Genet. 1997. PMID: 9182778 Review.

3

Increased need for medical interventions in infants with velocardiofacial (deletion 22q11) syndrome.

Hopkin RJ, Schorry EK, Bofinger M, Saal HM. Hopkin RJ, et al. J Pediatr. 2000 Aug;137(2):247-9. doi: 10.1067/mpd.2000.108272. J Pediatr. 2000. PMID: 10931419

4

Long-term survival in a patient with del(18)(q12.2q21.1).

Tinkle BT, Christianson CA, Schorry EK, Webb T, Hopkin RJ. Tinkle BT, et al. Among authors: hopkin rj. Am J Med Genet A. 2003 May 15;119A(1):66-70. doi: 10.1002/ajmg.a.10217. Am J Med Genet A. 2003. PMID: 12707962

5

Perception of disease severity in adolescents diagnosed with neurofibromatosis type 1.

Sebold CD, Lovell A, Hopkin R, Noll R, Schorry E. Sebold CD, et al. J Adolesc Health. 2004 Oct;35(4):297-302. doi: 10.1016/j.jadohealth.2003.10.003. J Adolesc Health. 2004. PMID: 15450543

6

Blood expression profiles for tuberous sclerosis complex 2, neurofibromatosis type 1, and Down's syndrome.

Tang Y, Schapiro MB, Franz DN, Patterson BJ, Hickey FJ, Schorry EK, Hopkin RJ, Wylie M, Narayan T, Glauser TA, Gilbert DL, Hershey AD, Sharp FR. Tang Y, et al. Among authors: hopkin rj. Ann Neurol. 2004 Dec;56(6):808-14. doi: 10.1002/ana.20291. Ann Neurol. 2004. PMID: 15562430

7

Human blood genomics: distinct profiles for gender, age and neurofibromatosis type 1.

Tang Y, Lu A, Ran R, Aronow BJ, Schorry EK, Hopkin RJ, Gilbert DL, Glauser TA, Hershey AD, Richtand NW, Privitera M, Dalvi A, Sahay A, Szaflarski JP, Ficker DM, Ratner N, Sharp FR. Tang Y, et al. Among authors: hopkin rj. Brain Res Mol Brain Res. 2004 Dec 20;132(2):155-67. doi: 10.1016/j.molbrainres.2003.10.014. Brain Res Mol Brain Res. 2004. PMID: 15582155

8

A new case of de novo 11q duplication in a patient with normal development and intelligence and review of the literature.

Zarate YA, Kogan JM, Schorry EK, Smolarek TA, Hopkin RJ. Zarate YA, et al. Among authors: hopkin rj. Am J Med Genet A. 2007 Feb 1;143A(3):265-70. doi: 10.1002/ajmg.a.31519. Am J Med Genet A. 2007. PMID: 17219392 Review.

9

Characterization of congenital anomalies in individuals with choanal atresia.

Burrow TA, Saal HM, de Alarcon A, Martin LJ, Cotton RT, Hopkin RJ. Burrow TA, et al. Among authors: hopkin rj. Arch Otolaryngol Head Neck Surg. 2009 Jun;135(6):543-7. doi: 10.1001/archoto.2009.53. Arch Otolaryngol Head Neck Surg. 2009. PMID: 19528400

10

Experience with hemihyperplasia and Beckwith-Wiedemann syndrome surveillance protocol.

Zarate YA, Mena R, Martin LJ, Steele P, Tinkle BT, Hopkin RJ. Zarate YA, et al. Among authors: hopkin rj. Am J Med Genet A. 2009 Aug;149A(8):1691-7. doi: 10.1002/ajmg.a.32966. Am J Med Genet A. 2009. PMID: 19610116

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