Summar ML - Search Results

1

Recurrent mutations in the vasopressin-neurophysin II gene cause autosomal dominant neurohypophyseal diabetes insipidus.

Repaske DR, Summar ML, Krishnamani MR, Gültekin EK, Arriazu MC, Roubicek ME, Blanco M, Isaac GB, Phillips JA 3rd. Repaske DR, et al. Among authors: summar ml. J Clin Endocrinol Metab. 1996 Jun;81(6):2328-34. doi: 10.1210/jcem.81.6.8964872. J Clin Endocrinol Metab. 1996. PMID: 8964872

2

Genetic mapping of the human pituitary-specific transcriptional factor gene and its analysis in familial panhypopituitary dwarfism.

Raskin S, Cogan JD, Summar ML, Moreno A, Krishnamani MR, Phillips JA 3rd. Raskin S, et al. Among authors: summar ml. Hum Genet. 1996 Dec;98(6):703-5. doi: 10.1007/s004390050289. Hum Genet. 1996. PMID: 8931705

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

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

8

Assignment of the human gene (GLCLR) that encodes the regulatory subunit of gamma-glutamylcysteine synthetase to chromosome 1p21.

Sierra-Rivera E, Dasouki M, Summar ML, Krishnamani MR, Meredith M, Rao PN, Phillips JA 3rd, Freeman ML. Sierra-Rivera E, et al. Among authors: summar ml. Cytogenet Cell Genet. 1996;72(2-3):252-4. doi: 10.1159/000134202. Cytogenet Cell Genet. 1996. PMID: 8978789

9

Heterogeneity in hereditary pancreatitis.

Dasouki MJ, Cogan J, Summar ML, Neblitt W 3rd, Foroud T, Koller D, Phillips JA 3rd. Dasouki MJ, et al. Among authors: summar ml. Am J Med Genet. 1998 Apr 28;77(1):47-53. Am J Med Genet. 1998. PMID: 9557894

10

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

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