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.
201 related articles for article (PubMed ID: 7328612)
1. Hereditary ectodermal dysplasia, olivopontocerebellar degeneration, short stature, and hypogonadism. Rushton AR; Genel M J Med Genet; 1981 Oct; 18(5):335-9. PubMed ID: 7328612 [TBL] [Abstract][Full Text] [Related]
2. Possible linkage between the Marinesco-Sjøgren syndrome and hypergonadotropic hypogonadism. Berg K; Skre H Cytogenet Cell Genet; 1976; 16(1-5):271-4. PubMed ID: 975888 [No Abstract] [Full Text] [Related]
3. Autosomal recessive syndrome of cerebellar ataxia and hypogonadotropic hypogonadism. Neuhäuser G; Opitz JM Clin Genet; 1975; 7(5):426-34. PubMed ID: 1149314 [TBL] [Abstract][Full Text] [Related]
4. Nonprogressive cerebellar disorder with mental retardation and autosomal recessive inheritance in Hutterites. Schurig V; Orman AV; Bowen P Am J Med Genet; 1981; 9(1):43-53. PubMed ID: 7246619 [TBL] [Abstract][Full Text] [Related]
5. Hypogonadotrophic hypogonadism, short stature, cerebellar ataxia, rod-cone retinal dystrophy, and hypersegmented neutrophils: a novel disorder or a new variant of Boucher-Neuhauser syndrome? Jbour AK; Mubaidin AF; Till M; El-Shanti H; Hadidi A; Ajlouni KM J Med Genet; 2003 Jan; 40(1):e2. PubMed ID: 12525550 [No Abstract] [Full Text] [Related]
6. Two brothers with Martsolf's syndrome. Sánchez JM; Barreiro C; Freilij H J Med Genet; 1985 Aug; 22(4):308-10. PubMed ID: 4045961 [TBL] [Abstract][Full Text] [Related]
7. Novel homozygous mutation, c.400C>T (p.Arg134*), in the PVRL1 gene underlies cleft lip/palate-ectodermal dysplasia syndrome in an Asian patient. Yoshida K; Hayashi R; Fujita H; Kubota M; Kondo M; Shimomura Y; Niizeki H J Dermatol; 2015 Jul; 42(7):715-9. PubMed ID: 25913853 [TBL] [Abstract][Full Text] [Related]
8. Linkage studies on Marinesco-Sjøgren syndrome and hypergonadotropic hypogonadism. Skre H; Berg K Clin Genet; 1977 Jan; 11(1):57-66. PubMed ID: 830450 [TBL] [Abstract][Full Text] [Related]
9. New autosomal recessive cerebellar ataxia disorder in a large inbred Lebanese family. Mégarbané A; Delague V; Ruchoux MM; Rizkallah E; Maurage CA; Viollet L; Rouaix-Emery N; Urtizberea A Am J Med Genet; 2001 Jun; 101(2):135-41. PubMed ID: 11391656 [TBL] [Abstract][Full Text] [Related]
10. Non-progressive cerebellar ataxia, aplasia of pupillary zone of iris, and mental subnormality (Gillespie's syndrome) affecting 3 members of a non-consanguineous family in 2 generations. Crawfurd MD; Harcourt RB; Shaw PA J Med Genet; 1979 Oct; 16(5):373-8. PubMed ID: 513084 [TBL] [Abstract][Full Text] [Related]
11. Multicore disease in sibs with severe mental retardation, short stature, facial anomalies, hypoplasia of the pituitary fossa, and hypogonadotrophic hypogonadism. Chudley AE; Rozdilsky B; Houston CS; Becker LE; Knoll JH Am J Med Genet; 1985 Jan; 20(1):145-58. PubMed ID: 3970066 [TBL] [Abstract][Full Text] [Related]
13. Mutations in GRHL2 result in an autosomal-recessive ectodermal Dysplasia syndrome. Petrof G; Nanda A; Howden J; Takeichi T; McMillan JR; Aristodemou S; Ozoemena L; Liu L; South AP; Pourreyron C; Dafou D; Proudfoot LE; Al-Ajmi H; Akiyama M; McLean WH; Simpson MA; Parsons M; McGrath JA Am J Hum Genet; 2014 Sep; 95(3):308-14. PubMed ID: 25152456 [TBL] [Abstract][Full Text] [Related]
14. New form of hidrotic ectodermal dysplasia in a Lebanese family. Mégarbané A; Noujeim Z; Fabre M; Der Kaloustian VM Am J Med Genet; 1998 Jan; 75(2):196-9. PubMed ID: 9450885 [TBL] [Abstract][Full Text] [Related]
15. A homozygous mutation of VWA3B causes cerebellar ataxia with intellectual disability. Kawarai T; Tajima A; Kuroda Y; Saji N; Orlacchio A; Terasawa H; Shimizu H; Kita Y; Izumi Y; Mitsui T; Imoto I; Kaji R J Neurol Neurosurg Psychiatry; 2016 Jun; 87(6):656-62. PubMed ID: 26157035 [TBL] [Abstract][Full Text] [Related]
16. A case of probable autosomal recessive ectodermal dysplasia with corkscrew hairs and mental retardation in a family with tuberous sclerosis. Argenziano G; Monsurrò MR; Pazienza R; Delfino M J Am Acad Dermatol; 1998 Feb; 38(2 Pt 2):344-8. PubMed ID: 9486713 [TBL] [Abstract][Full Text] [Related]
17. Familial cerebellar ataxia and hypogonadism associated with sensorimotor axonal polyneuropathy. Erdemoğlu AK; Akbostanci MC; Selçuki D Clin Neurol Neurosurg; 2000 Sep; 102(3):129-34. PubMed ID: 10996709 [TBL] [Abstract][Full Text] [Related]
18. [Neuroectodermal dysplasia in 2 Uzbek families]. Dadali EL; Ginter EK Zh Nevropatol Psikhiatr Im S S Korsakova; 1989; 89(2):58-61. PubMed ID: 2524944 [TBL] [Abstract][Full Text] [Related]