Garver KL - Search Results

1

Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22.

Puffenberger EG, Kauffman ER, Bolk S, Matise TC, Washington SS, Angrist M, Weissenbach J, Garver KL, Mascari M, Ladda R, et al. Puffenberger EG, et al. Among authors: garver kl. Hum Mol Genet. 1994 Aug;3(8):1217-25. doi: 10.1093/hmg/3.8.1217. Hum Mol Genet. 1994. PMID: 7987295

2

A genetic study of Hirschsprung disease.

Badner JA, Sieber WK, Garver KL, Chakravarti A. Badner JA, et al. Among authors: garver kl. Am J Hum Genet. 1990 Mar;46(3):568-80. Am J Hum Genet. 1990. PMID: 2309705 Free PMC article.

3

Cytogenetic studies in human sperm.

Estop AM, Cieply K, Vankirk V, Munne S, Garver K. Estop AM, et al. Hum Genet. 1991 Aug;87(4):447-51. doi: 10.1007/BF00197166. Hum Genet. 1991. PMID: 1879831

4

Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.

Lin AE, Garver KL, Diggans G, Clemens M, Wenger SL, Steele MW, Jones MC, Israel J. Lin AE, et al. Among authors: garver kl. Am J Med Genet. 1988 Nov;31(3):533-48. doi: 10.1002/ajmg.1320310308. Am J Med Genet. 1988. PMID: 3067575 Review.

5

The Human Genome Project and eugenic concerns.

Garver KL, Garver B. Garver KL, et al. Am J Hum Genet. 1994 Jan;54(1):148-58. Am J Hum Genet. 1994. PMID: 8279465 Free PMC article.

6

Update on MSAFP policy statement from the American Society of Human Genetics.

Garver KL. Garver KL. Am J Hum Genet. 1989 Aug;45(2):332-4. Am J Hum Genet. 1989. PMID: 2474250 Free PMC article. No abstract available.

7

Eugenics: past, present, and the future.

Garver KL, Garver B. Garver KL, et al. Am J Hum Genet. 1991 Nov;49(5):1109-18. Am J Hum Genet. 1991. PMID: 1928094 Free PMC article.

8

Hirschsprung disease: a genetic study.

Garver KL, Law JC, Garver B. Garver KL, et al. Among authors: garver b. Clin Genet. 1985 Dec;28(6):503-8. doi: 10.1111/j.1399-0004.1985.tb00417.x. Clin Genet. 1985. PMID: 2934185

9

Persistent hyperplastic primary vitreous with vertical transmission.

Lin AE, Biglan AW, Garver KL. Lin AE, et al. Among authors: garver kl. Ophthalmic Paediatr Genet. 1990 Jun;11(2):121-2. doi: 10.3109/13816819009012956. Ophthalmic Paediatr Genet. 1990. PMID: 2377350

10

Monozygotic Turner syndrome twins--correlation of phenotype severity and heart defect.

Lin AE, Garver KL. Lin AE, et al. Among authors: garver kl. Am J Med Genet. 1988 Mar;29(3):529-31. doi: 10.1002/ajmg.1320290309. Am J Med Genet. 1988. PMID: 3376996

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