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Year | Number of Results |
---|---|
1976 | 3 |
1977 | 2 |
1981 | 1 |
2024 | 0 |
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Page 1
The Sabinas syndrome.
Am J Hum Genet. 1981 Nov;33(6):957-67.
Am J Hum Genet. 1981.
PMID: 7325159
Free PMC article.
Ocular findings in mannosidosis.
Arbisser AI, Murphree AL, Garcia CA, Howell RR.
Arbisser AI, et al.
Am J Ophthalmol. 1976 Sep;82(3):465-71. doi: 10.1016/0002-9394(76)90496-7.
Am J Ophthalmol. 1976.
PMID: 961797
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Morquio-like syndrome with beta galactosidase deficiency and normal hexosamine sulfatase activity: mucopolysacchariodosis IVB.
Arbisser AI, Donnelly KA, Scott CI Jr, DiFerrante N, Singh J, Stevenson RE, Aylesworth AS, Howell RR.
Arbisser AI, et al.
Am J Med Genet. 1977;1(2):195-205. doi: 10.1002/ajmg.1320010205.
Am J Med Genet. 1977.
PMID: 416714
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A syndrome manifested by brittle hair with morphologic and biochemical abnormalities, developmental delay and normal stature.
Arbisser AI, Scott CI Jr, Howell RR, Ong PS, Cox HL Jr.
Arbisser AI, et al.
Birth Defects Orig Artic Ser. 1976;12(5):219-28.
Birth Defects Orig Artic Ser. 1976.
PMID: 953226
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Mesoectodermal dysgenesis: familial iris anomaly.
Drouilhet JH, Arbisser AI, Mazow ML.
Drouilhet JH, et al. Among authors: arbisser ai.
J Pediatr Ophthalmol. 1977 Nov-Dec;14(6):368-72.
J Pediatr Ophthalmol. 1977.
PMID: 604444
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Letter: Mannosidosis and maternal penicillamine therapy.
Arbisser AI, Scott CI Jr, Howell BR.
Arbisser AI, et al.
Lancet. 1976 Feb 7;1(7954):312-3. doi: 10.1016/s0140-6736(76)91454-9.
Lancet. 1976.
PMID: 55632
No abstract available.
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