83 related articles for article (PubMed ID: 953226)
1. A syndrome manifested by brittle hair with morphologic and biochemical abnormalities, developmental delay and normal stature.
Arbisser AI; Scott CI; Howell RR; Ong PS; Cox HL
Birth Defects Orig Artic Ser; 1976; 12(5):219-28. PubMed ID: 953226
[TBL] [Abstract][Full Text] [Related]
2. Trichothiodystrophy, mental retardation, short stature, ataxia, and gonadal dysfunction in three Moroccan siblings.
Przedborski S; Ferster A; Goldman S; Wolter R; Song M; Tonnesen T; Pollitt RJ; Vamos E
Am J Med Genet; 1990 Apr; 35(4):566-73. PubMed ID: 2333887
[TBL] [Abstract][Full Text] [Related]
3. Sabinas syndrome in monozygotic twins.
López-García DR; Salas-Alanis JC; Christiano AM; Ocampo-Candiani J; Gómez-Flores M
Clin Exp Dermatol; 2009 Jul; 34(5):e94-8. PubMed ID: 19438561
[TBL] [Abstract][Full Text] [Related]
4. Abnormal hair, craniofacial dysmorphism, and severe mental retardation - a new syndrome?
Killian W; Zonana J; Schroer RJ
J Clin Dysmorphol; 1983; 1(3):6-13. PubMed ID: 6584560
[No Abstract] [Full Text] [Related]
5. New autosomal recessive syndrome of sparse hair, osteopenia, and mental retardation in Mennonite sisters.
Kaler SG; Garrity AM; Stern HJ; Rosenbaum KN; Orrison BM; Marini JC; Bernardini I; Saal HM
Am J Med Genet; 1992 Aug; 43(6):983-8. PubMed ID: 1415349
[TBL] [Abstract][Full Text] [Related]
6. "Brittle" hair with short stature, intellectual impairment and decreased fertility: an autosomal recessive syndrome in an Amish kindred.
Jackson CE; Weiss L; Watson JH
Pediatrics; 1974 Aug; 54(2):201-7. PubMed ID: 4847854
[No Abstract] [Full Text] [Related]
7. Unknown syndrome in sibs: pili torti, growth delay, developmental delay, and mild neurological abnormalities.
Shapira SK; Neish AS; Pober BR
J Med Genet; 1992 Jul; 29(7):509-10. PubMed ID: 1379303
[TBL] [Abstract][Full Text] [Related]
8. [Trichothiodystrophy].
Meynadier J; Guillot B; Barnéon G; Djian B; Lévy A
Ann Dermatol Venereol; 1987; 114(12):1529-36. PubMed ID: 3445983
[TBL] [Abstract][Full Text] [Related]
9. Intermittent hair loss in a child with PIBI(D)S syndrome and trichothiodystrophy with defective DNA repair-xeroderma pigmentosum group D.
Kleijer WJ; Beemer FA; Boom BW
Am J Med Genet; 1994 Aug; 52(2):227-30. PubMed ID: 7802014
[TBL] [Abstract][Full Text] [Related]
10. Congenital hair defects.
Brown AC
Birth Defects Orig Artic Ser; 1971 Jun; 7(8):52-68. PubMed ID: 5173314
[TBL] [Abstract][Full Text] [Related]
11. Syndromes associated with trichothiodystrophy.
Tolmie JL; de Berker D; Dawber R; Galloway C; Gregory DW; Lehmann AR; McClure J; Pollitt RJ; Stephenson JB
Clin Dysmorphol; 1994 Jan; 3(1):1-14. PubMed ID: 8205320
[TBL] [Abstract][Full Text] [Related]
12. Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: a new X-linked mental retardation syndrome.
Chudley AE; Lowry RB; Hoar DI
Am J Med Genet; 1988 Dec; 31(4):741-51. PubMed ID: 3239563
[TBL] [Abstract][Full Text] [Related]
13. The KBG syndrome-a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomalies.
Herrmann J; Pallister PD; Tiddy W; Opitz JM
Birth Defects Orig Artic Ser; 1975; 11(5):7-18. PubMed ID: 1218237
[No Abstract] [Full Text] [Related]
14. A new X-linked multiple congenital anomalies/mental retardation syndrome.
Golabi M; Ito M; Hall BD
Am J Med Genet; 1984 Jan; 17(1):367-74. PubMed ID: 6711604
[TBL] [Abstract][Full Text] [Related]
15. [Kinky hair disease--a new syndrome with cerebral degeneration].
Neuhäuser G
Hippokrates; 1973 Oct; 44(3):316-8. PubMed ID: 4588328
[No Abstract] [Full Text] [Related]
16. [New hereditary syndrome with mental retardation].
Marincheva GS
Zh Nevropatol Psikhiatr Im S S Korsakova; 1990; 90(3):66-9. PubMed ID: 2163174
[TBL] [Abstract][Full Text] [Related]
17. Another family with tricho-rhino-phalangeal syndrome type III (Sugio-Kajii syndrome).
Nagai T; Nishimura G; Kasai H; Hasegawa T; Kato R; Ohashi H; Fukushima Y
Am J Med Genet; 1994 Feb; 49(3):278-80. PubMed ID: 8209886
[TBL] [Abstract][Full Text] [Related]
18. Teschler-Nicola/Killian syndrome.
Pagon RA
J Clin Dysmorphol; 1983; 1(3):18-9. PubMed ID: 6584556
[No Abstract] [Full Text] [Related]
19. A syndrome of facial dysmorphia, birth defects, myelodysplasia and immunodeficiency in three sibs of consanguineous parents.
Stoll C; Alembik Y; Lutz P
Genet Couns; 1994; 5(2):161-5. PubMed ID: 7917125
[TBL] [Abstract][Full Text] [Related]
20. Mental retardation, short stature, almond-shaped eyes, small downturned mouth and coned epiphyses: a new case of Hunter-Fraser syndrome.
Van Maldergem L; Gillerot Y; Perlmutter N; Wetzburger C; Koulischer L
Am J Med Genet; 1990 Oct; 37(2):283-5. PubMed ID: 2248298
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
