Lowry RB - Search Results

1

Borderline normal intelligence in the Smith-Lemli-Opitz (RSH) syndrome.

Lowry RB, Yong SL. Lowry RB, et al. Am J Med Genet. 1980;5(2):137-43. doi: 10.1002/ajmg.1320050205. Am J Med Genet. 1980. PMID: 7395908

2

Epiphyseal dysplasia, microcephaly, nystagmus, and retinitis pigmentosa.

Lowry RB, Wood BJ, Cox TA, Hayden MR. Lowry RB, et al. Am J Med Genet. 1989 Jul;33(3):341-5. doi: 10.1002/ajmg.1320330311. Am J Med Genet. 1989. PMID: 2801768

3

Alport syndrome and mental retardation: clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR).

Meloni I, Vitelli F, Pucci L, Lowry RB, Tonlorenzi R, Rossi E, Ventura M, Rizzoni G, Kashtan CE, Pober B, Renieri A. Meloni I, et al. Among authors: lowry rb. J Med Genet. 2002 May;39(5):359-65. doi: 10.1136/jmg.39.5.359. J Med Genet. 2002. PMID: 12011158 Free PMC article. No abstract available.

4

X-linked mental retardation with macro-orchidism and marker-X chromosomes.

Martin RH, Lin CC, Mathies BJ, Lowry RB. Martin RH, et al. Among authors: lowry rb. Am J Med Genet. 1980;7(4):433-41. doi: 10.1002/ajmg.1320070405. Am J Med Genet. 1980. PMID: 6938132

5

X linked alpha thalassaemia/mental retardation (ATR-X) syndrome.

Chudley AE, Lowry RB. Chudley AE, et al. Among authors: lowry rb. J Med Genet. 1992 May;29(5):357. doi: 10.1136/jmg.29.5.357. J Med Genet. 1992. PMID: 1583667 Free PMC article. No abstract available.

6

Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: a new X-linked mental retardation syndrome.

Chudley AE, Lowry RB, Hoar DI. Chudley AE, et al. Among authors: lowry rb. Am J Med Genet. 1988 Dec;31(4):741-51. doi: 10.1002/ajmg.1320310404. Am J Med Genet. 1988. PMID: 3239563

7

Clinical and mutational spectrum of Mowat-Wilson syndrome.

Zweier C, Thiel CT, Dufke A, Crow YJ, Meinecke P, Suri M, Ala-Mello S, Beemer F, Bernasconi S, Bianchi P, Bier A, Devriendt K, Dimitrov B, Firth H, Gallagher RC, Garavelli L, Gillessen-Kaesbach G, Hudgins L, Kääriäinen H, Karstens S, Krantz I, Mannhardt A, Medne L, Mücke J, Kibaek M, Krogh LN, Peippo M, Rittinger O, Schulz S, Schelley SL, Temple IK, Dennis NR, Van der Knaap MS, Wheeler P, Yerushalmi B, Zenker M, Seidel H, Lachmeijer A, Prescott T, Kraus C, Lowry RB, Rauch A. Zweier C, et al. Among authors: lowry rb. Eur J Med Genet. 2005 Apr-Jun;48(2):97-111. doi: 10.1016/j.ejmg.2005.01.003. Epub 2005 Feb 25. Eur J Med Genet. 2005. PMID: 16053902

8

Early onset of Cockayne syndrome.

Lowry RB. Lowry RB. Am J Med Genet. 1982 Oct;13(2):209-10. doi: 10.1002/ajmg.1320130211. Am J Med Genet. 1982. PMID: 7137232 No abstract available.

9

Survival and spectrum of anomalies in the Meckel syndrome.

Lowry RB, Hill RH, Tischler B. Lowry RB, et al. Am J Med Genet. 1983 Mar;14(3):417-21. doi: 10.1002/ajmg.1320140303. Am J Med Genet. 1983. PMID: 6859092

10

Keutel syndrome: clinical report and literature review.

Cormode EJ, Dawson M, Lowry RB. Cormode EJ, et al. Among authors: lowry rb. Am J Med Genet. 1986 Jun;24(2):289-94. doi: 10.1002/ajmg.1320240209. Am J Med Genet. 1986. PMID: 3717211

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