Ramer JC - Search Results

1

Congenital contractures, ectodermal dysplasia, cleft lip/palate, and developmental impairment: a distinct syndrome.

Ladda RL, Zonana J, Ramer JC, Mascari MJ, Rogan PK. Ladda RL, et al. Among authors: ramer jc. Am J Med Genet. 1993 Sep 15;47(4):550-5. doi: 10.1002/ajmg.1320470422. Am J Med Genet. 1993. PMID: 7504881

2

Cutaneous scar at anterior hair line in mother and child with associated frontal bone defect in child.

Stratis JP, Ramer JC, Manders EK, Lehman RA, Ladda RL. Stratis JP, et al. Among authors: ramer jc. Am J Med Genet. 1992 Sep 15;44(2):197-9. doi: 10.1002/ajmg.1320440215. Am J Med Genet. 1992. PMID: 1456291

3

Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: review of brain, cardiac, and limb malformations.

Ramer JC, Mowrey PN, Robins DB, Ligato S, Towfighi J, Ladda RL. Ramer JC, et al. Am J Med Genet. 1990 Nov;37(3):392-400. doi: 10.1002/ajmg.1320370320. Am J Med Genet. 1990. PMID: 2260571 Review.

4

A review of phenotype-karyotype correlations in individuals with interstitial deletions of the long arm of chromosome 2.

Ramer JC, Ladda RL, Frankel CA, Beckford A. Ramer JC, et al. Am J Med Genet. 1989 Mar;32(3):359-63. doi: 10.1002/ajmg.1320320318. Am J Med Genet. 1989. PMID: 2658585 Review.

5

Two infants with del(3)(p25pter) and a review of previously reported cases.

Ramer JC, Ladda RL, Frankel C. Ramer JC, et al. Am J Med Genet. 1989 May;33(1):108-12. doi: 10.1002/ajmg.1320330115. Am J Med Genet. 1989. PMID: 2665488 Review.

6

Humero-radial synostosis with ulnar defects in sibs.

Ramer JC, Ladda RL. Ramer JC, et al. Am J Med Genet. 1989 Jun;33(2):176-9. doi: 10.1002/ajmg.1320330207. Am J Med Genet. 1989. PMID: 2669480 Review.

7

Previously apparently undescribed syndrome: shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation.

Ramer JC, Lin AE, Dobyns WB, Winter R, Aymé S, Pallotta R, Ladda RL. Ramer JC, et al. Am J Med Genet. 1995 Jul 3;57(3):403-9. doi: 10.1002/ajmg.1320570308. Am J Med Genet. 1995. PMID: 7545868 Review.

8

Marden-Walker phenotype: spectrum of variability in three infants.

Ramer JC, Frankel CA, Ladda RL. Ramer JC, et al. Am J Med Genet. 1993 Feb 1;45(3):285-91. doi: 10.1002/ajmg.1320450302. Am J Med Genet. 1993. PMID: 7679543 Review.

9

Familial leuconychia, knuckle pads, hearing loss, and palmoplantar hyperkeratosis: an additional family with Bart-Pumphrey syndrome.

Ramer JC, Vasily DB, Ladda RL. Ramer JC, et al. J Med Genet. 1994 Jan;31(1):68-71. doi: 10.1136/jmg.31.1.68. J Med Genet. 1994. PMID: 8151643 Free PMC article.

10

Identical twins with Weissenbacher-Zweymüller syndrome and neural tube defect.

Ramer JC, Eggli K, Rogan PK, Ladda RL. Ramer JC, et al. Am J Med Genet. 1993 Mar 1;45(5):614-8. doi: 10.1002/ajmg.1320450520. Am J Med Genet. 1993. PMID: 8456835

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