These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
23. Genetics for the clinical obstetrician-gynecologist. Pernoll ML; King CR; Prescott GH Obstet Gynecol Annu; 1980; 9():1-53. PubMed ID: 7402500 [No Abstract] [Full Text] [Related]
24. [Clinical picture of X chromosome recessive ichthyosis]. Voss M Dermatol Monatsschr; 1985; 171(1):25-37. PubMed ID: 4038949 [No Abstract] [Full Text] [Related]
25. [Prenatal diagnosis of genetic disorders by linkage analysis (author's transl)]. Sperling K Wien Klin Wochenschr; 1982 Apr; 94(8):199-204. PubMed ID: 6954763 [TBL] [Abstract][Full Text] [Related]
26. The recurrence risks for isolated cases with incompletely penetrant X-linked conditions. Rogatko A Genet Epidemiol; 1986; 3(5):357-64. PubMed ID: 3781240 [TBL] [Abstract][Full Text] [Related]
27. Further linkage data on Norrie disease. Kivlin JD; Sanborn GE; Wright E; Cannon L; Carey J Am J Med Genet; 1987 Mar; 26(3):733-6. PubMed ID: 3565487 [TBL] [Abstract][Full Text] [Related]
28. [Presentation of a complex monitoring and therapy program in neuromuscular diseases, exemplified by X chromosomal muscular dystrophies. 2: Complex treatment concept]. Ullrich KP; Hoffmann W Padiatr Grenzgeb; 1987; 26(4):279-85. PubMed ID: 3658477 [No Abstract] [Full Text] [Related]
29. [Presentation of a complex monitoring and therapy program in neuromuscular diseases, exemplified by X chromosomal muscular dystrophies. 1: Etiology, development, clinical and paraclinical findings]. Hoffmann W; Ullrich KP Padiatr Grenzgeb; 1987; 26(4):271-8. PubMed ID: 3658476 [No Abstract] [Full Text] [Related]
30. [Genetic basis for Rett disease]. Midro AT; Panasiuk B Postepy Hig Med Dosw; 1997; 51(4):399-419. PubMed ID: 9446102 [TBL] [Abstract][Full Text] [Related]
31. Conference report: International Workshop on the fragile X and X-linked mental retardation. Opitz JM; Sutherland GR Am J Med Genet; 1984 Jan; 17(1):5-94. PubMed ID: 6369987 [No Abstract] [Full Text] [Related]
32. The X-linked infantile spasms syndrome (MIM 308350) maps to Xp11.4-Xpter in two pedigrees. Claes S; Devriendt K; Lagae L; Ceulemans B; Dom L; Casaer P; Raeymaekers P; Cassiman JJ; Fryns JP Ann Neurol; 1997 Sep; 42(3):360-4. PubMed ID: 9307258 [TBL] [Abstract][Full Text] [Related]
33. [Fertility and progeny of women with X-chromosome aberrations]. Rosenkranz W Wien Med Wochenschr; 1966 Apr; 116(15):334-5. PubMed ID: 5989476 [No Abstract] [Full Text] [Related]
34. [The type of inheritance of anhidrotic ectodermal dysplasia]. Al'tshuler BA; Suvorova KN Vestn Dermatol Venerol; 1984 Feb; (2):15-8. PubMed ID: 6720063 [No Abstract] [Full Text] [Related]
36. Diagnosis and treatment of a child with X-polysomy. Rustagi PK; Fine PM J Am Acad Child Adolesc Psychiatry; 1987 Jul; 26(4):593-4. PubMed ID: 3654518 [No Abstract] [Full Text] [Related]
37. Chromosome markers and mental retardation. Venter PA; Gericke GS S Afr Med J; 1981 Feb; 59(6):170. PubMed ID: 6936840 [No Abstract] [Full Text] [Related]
38. Genetic registers and the prevention of inherited disorders. Harper PS Proc Annu Symp Eugen Soc; 1983; 19():117-37. PubMed ID: 6230665 [No Abstract] [Full Text] [Related]
39. Hormone studies in patients with the Martin-Bell syndrome. Op't Hof J; Johnstone J; Venter PA S Afr Med J; 1983 Jan; 63(3):65. PubMed ID: 6681573 [No Abstract] [Full Text] [Related]