Summar ML - Search Results

1

Linkage analysis of the human dopamine beta-hydroxylase gene.

Perry SE, Summar ML, Phillips JA 3rd, Robertson D. Perry SE, et al. Among authors: summar ml. Genomics. 1991 Jun;10(2):493-5. doi: 10.1016/0888-7543(91)90339-g. Genomics. 1991. PMID: 2071155

2

The use of linkage analysis and the Centre d'Etude Polymorphisme Humain (CEPH) panel of DNA in the study of the arginine vasopressin, oxytocin and prodynorphin gene loci.

Summar ML. Summar ML. Prog Brain Res. 1992;93:309-17. doi: 10.1016/s0079-6123(08)64581-1. Prog Brain Res. 1992. PMID: 1362280 Review. No abstract available.

3

Linkage relationships of human arginine vasopressin-neurophysin-II and oxytocin-neurophysin-I to prodynorphin and other loci on chromosome 20.

Summar ML, Phillips JA 3rd, Battey J, Castiglione CM, Kidd KK, Maness KJ, Weiffenbach B, Gravius TC. Summar ML, et al. Mol Endocrinol. 1990 Jun;4(6):947-50. doi: 10.1210/mend-4-6-947. Mol Endocrinol. 1990. PMID: 1978246

4

Protein kinase C: a new linkage marker for growth hormone and for COL1A1.

Summar ML, Phillips JA 3rd, Krishnamani MR, Keefer J, Trofatter J, Schwartz RC, Tsipouras P, Willard H, Ullrich A. Summar ML, et al. Genomics. 1989 Jul;5(1):163-5. doi: 10.1016/0888-7543(89)90104-3. Genomics. 1989. PMID: 2570026

5

Physical and linkage mapping of human carbamyl phosphate synthetase I (CPS1) and reassignment from 2p to 2q35.

Summar ML, Dasouki MJ, Schofield PJ, Krishnamani MR, Vnencak-Jones C, Tuchman M, Mao J, Phillips JA 3rd. Summar ML, et al. Cytogenet Cell Genet. 1995;71(3):266-7. doi: 10.1159/000134124. Cytogenet Cell Genet. 1995. PMID: 7587391

6

Assignment of the gene (GLCLC) that encodes the heavy subunit of gamma-glutamylcysteine synthetase to human chromosome 6.

Sierra-Rivera E, Summar ML, Dasouki M, Krishnamani MR, Phillips JA, Freeman ML. Sierra-Rivera E, et al. Among authors: summar ml. Cytogenet Cell Genet. 1995;70(3-4):278-9. doi: 10.1159/000134051. Cytogenet Cell Genet. 1995. PMID: 7789189

7

Evidence that the Saethre-Chotzen syndrome locus lies between D7S664 and D7S507, by genetic analysis and detection of a microdeletion in a patient.

Lewanda AF, Green ED, Weissenbach J, Jerald H, Taylor E, Summar ML, Phillips JA 3rd, Cohen M, Feingold M, Mouradian W, et al. Lewanda AF, et al. Among authors: summar ml. Am J Hum Genet. 1994 Dec;55(6):1195-201. Am J Hum Genet. 1994. PMID: 7977380 Free PMC article.

8

Genetic mapping of the human growth hormone-releasing factor gene (GHRF) using two intragenic polymorphisms detected by PCR amplification.

Pérez Jurado LA, Phillips JA 3rd, Summar ML, Mao J, Weber JL, Schaefer FV, Hazan J, Argente J. Pérez Jurado LA, et al. Among authors: summar ml. Genomics. 1994 Mar 1;20(1):132-4. doi: 10.1006/geno.1994.1140. Genomics. 1994. PMID: 8020943

9

Linkage mapping of the gene for type III collagen (COL3A1) to human chromosome 2q using a VNTR polymorphism.

Tiller GE, Polumbo PA, Summar ML. Tiller GE, et al. Among authors: summar ml. Genomics. 1994 Mar 15;20(2):275-7. doi: 10.1006/geno.1994.1164. Genomics. 1994. PMID: 8020975

10

Angiotensin converting enzyme gene polymorphism: potential silencer motif and impact on progression in IgA nephropathy.

Hunley TE, Julian BA, Phillips JA 3rd, Summar ML, Yoshida H, Horn RG, Brown NJ, Fogo A, Ichikawa I, Kon V. Hunley TE, et al. Among authors: summar ml. Kidney Int. 1996 Feb;49(2):571-7. doi: 10.1038/ki.1996.81. Kidney Int. 1996. PMID: 8821846 Free article.

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