Berry-Kravis EM - Search Results

1

Sudden Infant Death Syndrome: review of implicated genetic factors.

Weese-Mayer DE, Ackerman MJ, Marazita ML, Berry-Kravis EM. Weese-Mayer DE, et al. Am J Med Genet A. 2007 Apr 15;143A(8):771-88. doi: 10.1002/ajmg.a.31722. Am J Med Genet A. 2007. PMID: 17340630 Review.

2

Two patients with overlapping de novo duplications of the long arm of chromosome 9, including one case with Di George sequence.

Lindgren V, Rosinsky B, Chin J, Berry-Kravis E. Lindgren V, et al. Am J Med Genet. 1994 Jan 1;49(1):67-73. doi: 10.1002/ajmg.1320490112. Am J Med Genet. 1994. PMID: 8172253

3

Demonstration of abnormal cyclic AMP production in platelets from patients with fragile X syndrome.

Berry-Kravis E, Sklena P. Berry-Kravis E, et al. Am J Med Genet. 1993 Jan 1;45(1):81-7. doi: 10.1002/ajmg.1320450120. Am J Med Genet. 1993. PMID: 8380312

4

Mosaic trisomy 16 ascertained through amniocentesis: evaluation of 11 new cases.

Hsu WT, Shchepin DA, Mao R, Berry-Kravis E, Garber AP, Fischel-Ghodsian N, Falk RE, Carlson DE, Roeder ER, Leeth EA, Hajianpour MJ, Wang JC, Rosenblum-Vos LS, Bhatt SD, Karson EM, Hux CH, Trunca C, Bialer MG, Linn SK, Schreck RR. Hsu WT, et al. Am J Med Genet. 1998 Dec 28;80(5):473-80. doi: 10.1002/(sici)1096-8628(19981228)80:5<473::aid-ajmg7>3.0.co;2-a. Am J Med Genet. 1998. PMID: 9880211

5

X-linked lissencephaly with absent corpus callosum and ambiguous genitalia.

Dobyns WB, Berry-Kravis E, Havernick NJ, Holden KR, Viskochil D. Dobyns WB, et al. Am J Med Genet. 1999 Oct 8;86(4):331-7. Am J Med Genet. 1999. PMID: 10494089 Review.

6

Epilepsy in fragile X syndrome.

Berry-Kravis E. Berry-Kravis E. Dev Med Child Neurol. 2002 Nov;44(11):724-8. doi: 10.1017/s0012162201002833. Dev Med Child Neurol. 2002. PMID: 12418611

7

Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter gene.

Weese-Mayer DE, Berry-Kravis EM, Maher BS, Silvestri JM, Curran ME, Marazita ML. Weese-Mayer DE, et al. Am J Med Genet A. 2003 Mar 15;117A(3):268-74. doi: 10.1002/ajmg.a.20005. Am J Med Genet A. 2003. PMID: 12599191

8

Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis.

Weese-Mayer DE, Zhou L, Berry-Kravis EM, Maher BS, Silvestri JM, Marazita ML. Weese-Mayer DE, et al. Am J Med Genet A. 2003 Oct 15;122A(3):238-45. doi: 10.1002/ajmg.a.20427. Am J Med Genet A. 2003. PMID: 12966525

9

Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b.

Weese-Mayer DE, Berry-Kravis EM, Zhou L, Maher BS, Silvestri JM, Curran ME, Marazita ML. Weese-Mayer DE, et al. Am J Med Genet A. 2003 Dec 15;123A(3):267-78. doi: 10.1002/ajmg.a.20527. Am J Med Genet A. 2003. PMID: 14608649

10

Psychopharmacology in fragile X syndrome--present and future.

Berry-Kravis E, Potanos K. Berry-Kravis E, et al. Ment Retard Dev Disabil Res Rev. 2004;10(1):42-8. doi: 10.1002/mrdd.20007. Ment Retard Dev Disabil Res Rev. 2004. PMID: 14994287 Review.

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