Ladda RL - Search Results

1

Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia.

Rogan PK, Close P, Blouin JL, Seip JR, Gannutz L, Ladda RL, Antonarakis SE. Rogan PK, et al. Among authors: ladda rl. Am J Med Genet. 1995 Nov 6;59(2):174-81. doi: 10.1002/ajmg.1320590212. Am J Med Genet. 1995. PMID: 8588582

2

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. Am J Med Genet. 1993 Sep 15;47(4):550-5. doi: 10.1002/ajmg.1320470422. Am J Med Genet. 1993. PMID: 7504881

3

Clinical and molecular analyses of deletion 3p25-pter syndrome.

Mowrey PN, Chorney MJ, Venditti CP, Latif F, Modi WS, Lerman MI, Zbar B, Robins DB, Rogan PK, Ladda RL. Mowrey PN, et al. Among authors: ladda rl. Am J Med Genet. 1993 Jul 1;46(6):623-9. doi: 10.1002/ajmg.1320460604. Am J Med Genet. 1993. PMID: 8103286

4

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

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

5

A new missense mutation, Arg719Gln, in the beta-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy.

Consevage MW, Salada GC, Baylen BG, Ladda RL, Rogan PK. Consevage MW, et al. Among authors: ladda rl. Hum Mol Genet. 1994 Jun;3(6):1025-6. doi: 10.1093/hmg/3.6.1025. Hum Mol Genet. 1994. PMID: 7848441 No abstract available.

6

Absence of linkage of apparently single gene mediated ADHD with the human syntenic region of the mouse mutant Coloboma.

Hess EJ, Rogan PK, Domoto M, Tinker DE, Ladda RL, Ramer JC. Hess EJ, et al. Among authors: ladda rl. Am J Med Genet. 1995 Dec 18;60(6):573-9. doi: 10.1002/ajmg.1320600619. Am J Med Genet. 1995. PMID: 8825900

7

The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

Mascari MJ, Gottlieb W, Rogan PK, Butler MG, Waller DA, Armour JA, Jeffreys AJ, Ladda RL, Nicholls RD. Mascari MJ, et al. Among authors: ladda rl. N Engl J Med. 1992 Jun 11;326(24):1599-607. doi: 10.1056/NEJM199206113262404. N Engl J Med. 1992. PMID: 1584261 Free PMC article.

8

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. Among authors: ladda rl. Am J Med Genet. 1990 Nov;37(3):392-400. doi: 10.1002/ajmg.1320370320. Am J Med Genet. 1990. PMID: 2260571 Review.

9

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. Among authors: ladda rl. Am J Med Genet. 1989 Mar;32(3):359-63. doi: 10.1002/ajmg.1320320318. Am J Med Genet. 1989. PMID: 2658585 Review.

10

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

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

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