Wenger S - Search Results

1

Lack of mitogenic effects of growth hormone on human leukemic lymphoblasts.

Blatt J, Wenger S, Stitely S, Lee PA. Blatt J, et al. Among authors: wenger s. Eur J Pediatr. 1987 May;146(3):257-60. doi: 10.1007/BF00716469. Eur J Pediatr. 1987. PMID: 3474148

2

Pancytopenia and vacuolation of marrow precursors associated with necrotizing encephalopathy.

Blatt J, Katerji A, Barmada M, Wenger SL, Penchansky L. Blatt J, et al. Among authors: wenger sl. Br J Haematol. 1994 Jan;86(1):207-9. doi: 10.1111/j.1365-2141.1994.tb03280.x. Br J Haematol. 1994. PMID: 8011533

3

46XY siblings with inadequate virilization and CNS deficiency.

Hoffman RP, Steele MW, Lee PA, Brown TR, Wenger SL, Skiba PL. Hoffman RP, et al. Among authors: wenger sl. Horm Res. 1988;29(5-6):207-10. doi: 10.1159/000181004. Horm Res. 1988. PMID: 3220458

4

Detection of Y chromosome sequences in Turner's syndrome by Southern blot analysis of amplified DNA.

Kocova M, Siegel SF, Wenger SL, Lee PA, Trucco M. Kocova M, et al. Among authors: wenger sl. Lancet. 1993 Jul 17;342(8864):140-3. doi: 10.1016/0140-6736(93)91345-m. Lancet. 1993. PMID: 8101256

5

Rhabdomyosarcoma in Roberts syndrome.

Wenger SL, Blatt J, Steele MW, Lloyd DA, Bellinger M, Phebus CK, Horn M, Jaffe R. Wenger SL, et al. Cancer Genet Cytogenet. 1988 Apr;31(2):285-9. doi: 10.1016/0165-4608(88)90230-0. Cancer Genet Cytogenet. 1988. PMID: 3349442

6

Detection of Y chromosome sequences in a 45,X/46,XXq--patient by Southern blot analysis of PCR-amplified DNA and fluorescent in situ hybridization (FISH).

Kocova M, Siegel SF, Wenger SL, Lee PA, Nalesnik M, Trucco M. Kocova M, et al. Among authors: wenger sl. Am J Med Genet. 1995 Feb 13;55(4):483-8. doi: 10.1002/ajmg.1320550418. Am J Med Genet. 1995. PMID: 7762591

7

A simplified six-item checklist for screening for fragile X syndrome in the pediatric population.

Giangreco CA, Steele MW, Aston CE, Cummins JH, Wenger SL. Giangreco CA, et al. Among authors: wenger sl. J Pediatr. 1996 Oct;129(4):611-4. doi: 10.1016/s0022-3476(96)70130-0. J Pediatr. 1996. PMID: 8859272

8

Trisomy 18 syndrome in a full-term liveborn after in vitro fertilization.

Steele MW, Wenger SL. Steele MW, et al. Among authors: wenger sl. Fertil Steril. 1987 Jul;48(1):162. doi: 10.1016/s0015-0282(16)59310-8. Fertil Steril. 1987. PMID: 3595912 Free article. No abstract available.

9

The fragile X marker and autism in perspective.

Payton JB, Steele MW, Wenger SL, Minshew NJ. Payton JB, et al. Among authors: wenger sl. J Am Acad Child Adolesc Psychiatry. 1989 May;28(3):417-21. doi: 10.1097/00004583-198905000-00019. J Am Acad Child Adolesc Psychiatry. 1989. PMID: 2738009

10

Incorporation of bacteriophage DNA into the genome of cultured human lymphocytes.

Wenger SL, Steele MW, Turner JH. Wenger SL, et al. In Vitro. 1981 Aug;17(8):695-700. doi: 10.1007/BF02628405. In Vitro. 1981. PMID: 7327598

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