Moss E - Search Results

1

Communication disorders in the 22Q11.2 microdeletion syndrome.

Solot CB, Knightly C, Handler SD, Gerdes M, McDonald-McGinn DM, Moss E, Wang P, Cohen M, Randall P, Larossa D, Driscoll DA. Solot CB, et al. Among authors: moss e. J Commun Disord. 2000 May-Jun;33(3):187-203; quiz 203-4. doi: 10.1016/s0021-9924(00)00018-6. J Commun Disord. 2000. PMID: 10907715

2

Developmental presentation of 22q11.2 deletion (DiGeorge/velocardiofacial syndrome).

Wang PP, Solot C, Moss EM, Gerdes M, McDonald-McGinn DM, Driscoll DA, Emanuel BS, Zackai EH. Wang PP, et al. Among authors: moss em. J Dev Behav Pediatr. 1998 Oct;19(5):342-5. doi: 10.1097/00004703-199810000-00004. J Dev Behav Pediatr. 1998. PMID: 9809264 No abstract available.

3

Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.

Moss EM, Batshaw ML, Solot CB, Gerdes M, McDonald-McGinn DM, Driscoll DA, Emanuel BS, Zackai EH, Wang PP. Moss EM, et al. J Pediatr. 1999 Feb;134(2):193-8. doi: 10.1016/s0022-3476(99)70415-4. J Pediatr. 1999. PMID: 9931529

4

The Philadelphia story: the 22q11.2 deletion: report on 250 patients.

McDonald-McGinn DM, Kirschner R, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Solot C, Wang P, Jacobs I, Handler S, Knightly C, Heher K, Wilson M, Ming JE, Grace K, Driscoll D, Pasquariello P, Randall P, Larossa D, Emanuel BS, Zackai EH. McDonald-McGinn DM, et al. Among authors: moss e. Genet Couns. 1999;10(1):11-24. Genet Couns. 1999. PMID: 10191425

5

Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion.

Gerdes M, Solot C, Wang PP, Moss E, LaRossa D, Randall P, Goldmuntz E, Clark BJ 3rd, Driscoll DA, Jawad A, Emanuel BS, McDonald-McGinn DM, Batshaw ML, Zackai EH. Gerdes M, et al. Among authors: moss e. Am J Med Genet. 1999 Jul 16;85(2):127-33. Am J Med Genet. 1999. PMID: 10406665

6

The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients.

McDonald-McGinn DM, LaRossa D, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Wang P, Solot C, Schultz P, Lynch D, Bingham P, Keenan G, Weinzimer S, Ming JE, Driscoll D, Clark BJ 3rd, Markowitz R, Cohen A, Moshang T, Pasquariello P, Randall P, Emanuel BS, Zackai EH. McDonald-McGinn DM, et al. Among authors: moss e. Genet Test. 1997;1(2):99-108. doi: 10.1089/gte.1997.1.99. Genet Test. 1997. PMID: 10464633

7

Neurodevelopmental outcome and lifestyle assessment in school-aged and adolescent children with hypoplastic left heart syndrome.

Mahle WT, Clancy RR, Moss EM, Gerdes M, Jobes DR, Wernovsky G. Mahle WT, et al. Among authors: moss em. Pediatrics. 2000 May;105(5):1082-9. doi: 10.1542/peds.105.5.1082. Pediatrics. 2000. PMID: 10790466

8

Morphometry of the head of the caudate nucleus in patients with velocardiofacial syndrome (del 22q11.2).

Sugama S, Bingham PM, Wang PP, Moss EM, Kobayashi H, Eto Y. Sugama S, et al. Among authors: moss em. Acta Paediatr. 2000 May;89(5):546-9. doi: 10.1080/080352500750027826. Acta Paediatr. 2000. PMID: 10852189

9

Research on behavioral phenotypes: velocardiofacial syndrome (deletion 22q11.2).

Wang PP, Woodin MF, Kreps-Falk R, Moss EM. Wang PP, et al. Among authors: moss em. Dev Med Child Neurol. 2000 Jun;42(6):422-7. doi: 10.1017/s0012162200000785. Dev Med Child Neurol. 2000. PMID: 10875531 Free article. Review. No abstract available.

10

Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion.

Woodin M, Wang PP, Aleman D, McDonald-McGinn D, Zackai E, Moss E. Woodin M, et al. Among authors: moss e. Genet Med. 2001 Jan-Feb;3(1):34-9. doi: 10.1097/00125817-200101000-00008. Genet Med. 2001. PMID: 11339375 Free article.

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