Cunniff C - Search Results

1

Autosomal dominant benign neonatal seizures.

Cunniff C, Wiedlin N, Jones KL. Cunniff C, et al. Am J Med Genet. 1988 Aug;30(4):963-6. doi: 10.1002/ajmg.1320300414. Am J Med Genet. 1988. PMID: 3189416

2

Pentalogy of Cantrell and ectopia cordis, a familial developmental field complex.

Martin RA, Cunniff C, Erickson L, Jones KL. Martin RA, et al. Among authors: cunniff c. Am J Med Genet. 1992 Apr 1;42(6):839-41. doi: 10.1002/ajmg.1320420619. Am J Med Genet. 1992. PMID: 1554024

3

Interstitial deletion of chromosome 2q associated with ovarian dysgenesis.

Davis E, Grafe M, Cunniff C, Jones KL, Bogart M. Davis E, et al. Among authors: cunniff c. Clin Genet. 1991 May;39(5):386-90. doi: 10.1111/j.1399-0004.1991.tb03047.x. Clin Genet. 1991. PMID: 1860256

4

Ovarian dysgenesis in individuals with chromosomal abnormalities.

Cunniff C, Jones KL, Benirschke K. Cunniff C, et al. Hum Genet. 1991 Apr;86(6):552-6. doi: 10.1007/BF00201540. Hum Genet. 1991. PMID: 2026420

5

Craniosynostosis and lid anomalies: report of a girl with Michels syndrome.

Cunniff C, Jones KL. Cunniff C, et al. Am J Med Genet. 1990 Sep;37(1):28-30. doi: 10.1002/ajmg.1320370108. Am J Med Genet. 1990. PMID: 2240039

6

Patterns of malformation in children with congenital diaphragmatic defects.

Cunniff C, Jones KL, Jones MC. Cunniff C, et al. J Pediatr. 1990 Feb;116(2):258-61. doi: 10.1016/s0022-3476(05)82884-7. J Pediatr. 1990. PMID: 2299497

7

Oligohydramnios sequence and renal tubular malformation associated with maternal enalapril use.

Cunniff C, Jones KL, Phillipson J, Benirschke K, Short S, Wujek J. Cunniff C, et al. Am J Obstet Gynecol. 1990 Jan;162(1):187-9. doi: 10.1016/0002-9378(90)90846-y. Am J Obstet Gynecol. 1990. PMID: 2301491

8

Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia.

Cunniff C, Jones KL, Saal HM, Stern HJ. Cunniff C, et al. Pediatrics. 1990 Apr;85(4):499-504. Pediatrics. 1990. PMID: 2314962

9

Terminal deletions of the long arm of chromosome 7: five new cases.

Bogart MH, Cunniff C, Bradshaw C, Jones KL, Jones OW. Bogart MH, et al. Among authors: cunniff c. Am J Med Genet. 1990 May;36(1):53-5. doi: 10.1002/ajmg.1320360112. Am J Med Genet. 1990. PMID: 2333907

10

Chromosome 10qter deletion syndrome: a review and report of three new cases.

Wulfsberg EA, Weaver RP, Cunniff CM, Jones MC, Jones KL. Wulfsberg EA, et al. Among authors: cunniff cm. Am J Med Genet. 1989 Mar;32(3):364-7. doi: 10.1002/ajmg.1320320319. Am J Med Genet. 1989. PMID: 2658586 Review.

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