138 related articles for article (PubMed ID: 5516239)
1. Amish albinism: a distinctive autosomal recessive phenotype.
Nance WE; Jackson CE; Witkop CJ
Am J Hum Genet; 1970 Sep; 22(5):579-86. PubMed ID: 5516239
[No Abstract] [Full Text] [Related]
2. Albinism in England.
Jay B; Witkop CJ; King RA
Birth Defects Orig Artic Ser; 1982; 18(6):319-25. PubMed ID: 6816306
[No Abstract] [Full Text] [Related]
3. X-linked ocular albinism: a family containing a manifesting heterozygote, and an affected male married to a female with autosomal recessive ocular albinism.
Jaeger C; Jay B
Hum Genet; 1981; 56(3):299-304. PubMed ID: 7239514
[TBL] [Abstract][Full Text] [Related]
4. Albinism, or the NOACH syndrome (the book of Enoch c.v. 1-20).
van Dorp DB
Clin Genet; 1987 Apr; 31(4):228-42. PubMed ID: 3109790
[TBL] [Abstract][Full Text] [Related]
5. [Studies of X-linked recessive ocular albinism of the Nettleship-Falls type--with special reference to the association of megalocornea].
Awaya S; Tsunekawa F; Koizumi E; Miyake Y; Yokoyama K
Nippon Ganka Gakkai Zasshi; 1988 Jan; 92(1):146-50. PubMed ID: 3389256
[No Abstract] [Full Text] [Related]
6. Autosomal recessive oculocutaneous albinism in man. Evidence for genetic heterogeneity.
Witkop CJ; Nance WE; Rawls RF; White JG
Am J Hum Genet; 1970 Jan; 22(1):55-74. PubMed ID: 4983623
[No Abstract] [Full Text] [Related]
7. Albinism.
François J
Ophthalmologica; 1979; 178(1-2):19-31. PubMed ID: 108645
[TBL] [Abstract][Full Text] [Related]
8. [Albinism in certain clinical and genetic arieties. Study and research on a family].
Morra M
Minerva Oftalmol; 1967; 9(6):202-5. PubMed ID: 5617749
[No Abstract] [Full Text] [Related]
9. [Study on genetic epidemiology of albinism].
Gong Y; Shao C; Zheng H; Chen B; Guo Y
Yi Chuan Xue Bao; 1994; 21(3):169-72. PubMed ID: 7917429
[TBL] [Abstract][Full Text] [Related]
10. Autosomal recessively inherited ocular albinism. A new form of ocular albinism affecting females as severely as males.
O'Donnell FE; King RA; Green WR; Witkop CJ
Arch Ophthalmol; 1978 Sep; 96(9):1621-5. PubMed ID: 687204
[TBL] [Abstract][Full Text] [Related]
11. Genetic and biochemical evidence for two forms of oculocutaneous albinism in man.
Nance WE; Witkop CJ; Rawls RF
Birth Defects Orig Artic Ser; 1971 Mar; 7(3):125-8. PubMed ID: 5173133
[TBL] [Abstract][Full Text] [Related]
12. [Ethnic variation in congenital pigmentation anomalies].
Eckes LK
Hautarzt; 1980 Oct; 31(10):531-9. PubMed ID: 7451134
[TBL] [Abstract][Full Text] [Related]
13. Segregation analysis of brown oculocutaneous albinism.
King RA; Rich SS
Clin Genet; 1986 Jun; 29(6):496-501. PubMed ID: 3742854
[TBL] [Abstract][Full Text] [Related]
14. Recessive albinism in three children and both parents.
Oliver M; Fried K
J Med Genet; 1970 Jun; 7(2):153-4. PubMed ID: 4933409
[No Abstract] [Full Text] [Related]
15. [Griscelli-Prunieras syndrome: report of two cases].
González Carretero P; Noguera Julian A; Ricart Campos S; Fortuny Guasch C; Martorell Sampol L
An Pediatr (Barc); 2009 Feb; 70(2):164-7. PubMed ID: 19217573
[TBL] [Abstract][Full Text] [Related]
16. Hereditary congenital severe deafness syndromes.
Konigsmark BW
Ann Otol Rhinol Laryngol; 1971 Apr; 80(2):269-88. PubMed ID: 4927796
[No Abstract] [Full Text] [Related]
17. The molecular basis of type I (tyrosinase-deficient) human oculocutaneous albinism.
Giebel LB; Spritz RA
Pigment Cell Res; 1992; Suppl 2():101-6. PubMed ID: 1409411
[No Abstract] [Full Text] [Related]
18. Homozygosity in piebald trait.
Hultén MA; Honeyman MM; Mayne AJ; Tarlow MJ
J Med Genet; 1987 Sep; 24(9):568-71. PubMed ID: 3669051
[TBL] [Abstract][Full Text] [Related]
19. A novel deletion mutation in the ALOX12B gene in a Kurdish family with autosomal recessive congenital ichthyosis.
Lolas IB; Sommerlund M; Okkels H; Ramsing M; Petersen MB
J Eur Acad Dermatol Venereol; 2016 Nov; 30(11):e144-e145. PubMed ID: 26575587
[No Abstract] [Full Text] [Related]
20. Albinism: modern molecular diagnosis.
Carden SM; Boissy RE; Schoettker PJ; Good WV
Br J Ophthalmol; 1998 Feb; 82(2):189-95. PubMed ID: 9613388
[No Abstract] [Full Text] [Related]
[Next] [New Search]
