Moore CA - Search Results

1

Asymmetric and symmetric long bone bowing in two sibs: an apparently new bone dysplasia.

Moore LA, Moore CA, Smith JA, Weaver DD. Moore LA, et al. Among authors: moore ca. Am J Med Genet. 1993 Nov 15;47(7):1072-7. doi: 10.1002/ajmg.1320470728. Am J Med Genet. 1993. PMID: 8291526

2

Familial occurrence of renal and Müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay.

Davee MA, Moore CA, Bull MJ, Hodes ME. Davee MA, et al. Among authors: moore ca. Am J Med Genet. 1992 Oct 1;44(3):293-6. doi: 10.1002/ajmg.1320440306. Am J Med Genet. 1992. PMID: 1283287

3

Fetal brain disruption sequence.

Moore CA, Weaver DD, Bull MJ. Moore CA, et al. J Pediatr. 1990 Mar;116(3):383-6. doi: 10.1016/s0022-3476(05)82825-2. J Pediatr. 1990. PMID: 2308027

4

Familial distal arthrogryposis with craniofacial abnormalities: a new subtype of type II?

Moore CA, Weaver DD. Moore CA, et al. Am J Med Genet. 1989 Jun;33(2):231-7. doi: 10.1002/ajmg.1320330218. Am J Med Genet. 1989. PMID: 2764034

5

Acephalus-acardia in twins with aneuploidy.

Moore CA, Buehler BA, McManus BM, Harmon JP, Mirkin LD, Goldstein DJ. Moore CA, et al. Am J Med Genet Suppl. 1987;3:139-43. doi: 10.1002/ajmg.1320280516. Am J Med Genet Suppl. 1987. PMID: 3130847 Review.

6

Neural tube defects and omphalocele in trisomy 18.

Moore CA, Harmon JP, Padilla LM, Castro VB, Weaver DD. Moore CA, et al. Clin Genet. 1988 Aug;34(2):98-103. doi: 10.1111/j.1399-0004.1988.tb02843.x. Clin Genet. 1988. PMID: 3191615

7

Otopalatodigital syndrome type II associated with omphalocele: report of three cases.

Young K, Barth CK, Moore C, Weaver DD. Young K, et al. Am J Med Genet. 1993 Feb 15;45(4):481-7. doi: 10.1002/ajmg.1320450418. Am J Med Genet. 1993. PMID: 8465856

8

Macrocephaly-cutis marmorata telangiectatica congenita: a distinct disorder with developmental delay and connective tissue abnormalities.

Moore CA, Toriello HV, Abuelo DN, Bull MJ, Curry CJ, Hall BD, Higgins JV, Stevens CA, Twersky S, Weksberg R, Dobyns WB. Moore CA, et al. Am J Med Genet. 1997 May 2;70(1):67-73. Am J Med Genet. 1997. PMID: 9129744

9

Mild autosomal dominant hypophosphatasia: in utero presentation in two families.

Moore CA, Curry CJ, Henthorn PS, Smith JA, Smith JC, O'Lague P, Coburn SP, Weaver DD, Whyte MP. Moore CA, et al. Am J Med Genet. 1999 Oct 29;86(5):410-5. doi: 10.1002/(sici)1096-8628(19991029)86:5<410::aid-ajmg3>3.0.co;2-0. Am J Med Genet. 1999. PMID: 10508980

10

Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexia.

Abidi FE, Holloway L, Moore CA, Weaver DD, Simensen RJ, Stevenson RE, Rogers RC, Schwartz CE. Abidi FE, et al. Among authors: moore ca. J Med Genet. 2008 Dec;45(12):787-93. doi: 10.1136/jmg.2008.058990. Epub 2008 Aug 12. J Med Genet. 2008. PMID: 18697827 Free PMC article.

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