PubMed (cited) for id: 310600

Year	Number of Results
1922	1
1937	1
1940	1
1947	1
1949	1
1956	1
1958	1
1959	1
1961	1
1963	1
1965	1
1966	1
1969	1
1971	1
1979	1
1982	1
1985	3
1986	3
1987	1
1988	5
1989	6
1992	8
1993	3
1995	4
1997	1
2007	1
2024	0

1

Sex-linked Microphthalmia and Mental Deficiency.

Roberts JA. Roberts JA. Br Med J. 1937 Dec 18;2(4015):1213-6. doi: 10.1136/bmj.2.4015.1213. Br Med J. 1937. PMID: 20781115 Free PMC article. No abstract available.

2

HEREDITARY MICROPHTHALMIA.

Ash WM. Ash WM. Br Med J. 1922 Apr 8;1(3197):558-9. doi: 10.1136/bmj.1.3197.558. Br Med J. 1922. PMID: 20770671 Free PMC article. No abstract available.

3

A case of sex-linked microphthalmia.

STEPHENS FE. STEPHENS FE. J Hered. 1947 Oct;38(10):306-10. J Hered. 1947. PMID: 18900295 No abstract available.

4

MICROPHTHALMIA AND THE VISUAL PATHWAYS: A Case Associated with Blindness and Imbecility, and Sex-linked.

Whitnall SE, Norman RM. Whitnall SE, et al. Br J Ophthalmol. 1940 May;24(5):229-44. doi: 10.1136/bjo.24.5.229. Br J Ophthalmol. 1940. PMID: 18169694 Free PMC article. No abstract available.

5

Congenital blindness (pseudoglioma) occurring as a sex-linked developmental anomaly.

WILSON WM. WILSON WM. Can Med Assoc J. 1949 Jun;60(6):580-4. Can Med Assoc J. 1949. PMID: 18134442 Free PMC article. No abstract available.

6

A novel missense mutation in the NDP gene in a child with Norrie disease and severe neurological involvement including infantile spasms.

Lev D, Weigl Y, Hasan M, Gak E, Davidovich M, Vinkler C, Leshinsky-Silver E, Lerman-Sagie T, Watemberg N. Lev D, et al. Am J Med Genet A. 2007 May 1;143A(9):921-4. doi: 10.1002/ajmg.a.31531. Am J Med Genet A. 2007. PMID: 17334993

7

NORRIE'S DISEASE AND THE XG BLOOD GROUP SYSTEM: LINKAGE DATA.

WARBURG M, HAUGE M, SANGER R. WARBURG M, et al. Acta Genet Stat Med. 1965;15:103-15. doi: 10.1159/000151898. Acta Genet Stat Med. 1965. PMID: 14300021 No abstract available.

8

Norie's disease (atrofia bulborum hereditaria).

WARBURG M. WARBURG M. Acta Ophthalmol (Copenh). 1963;41:134-46. doi: 10.1111/j.1755-3768.1963.tb03533.x. Acta Ophthalmol (Copenh). 1963. PMID: 13998843 No abstract available.

9

Norrie's disease: congenital bilateral pseudotumor of the retina with recessive X-chromosomal inheritance; preliminary report.

ANDERSEN SR, WARBURG M. ANDERSEN SR, et al. Arch Ophthalmol. 1961 Nov;66:614-8. doi: 10.1001/archopht.1961.00960010616003. Arch Ophthalmol. 1961. PMID: 13861187 No abstract available.

10

Episkopi blindness; hereditary blindness in a Greek Cypriot family.

TAYLOR PJ, COATES T, NEWHOUSE ML. TAYLOR PJ, et al. Br J Ophthalmol. 1959 Jun;43(6):340-4. doi: 10.1136/bjo.43.6.340. Br J Ophthalmol. 1959. PMID: 13662558 Free PMC article. No abstract available.

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