254 related articles for article (PubMed ID: 7943046)
1. X-linked mental retardation, microcephaly, and growth delay associated with hereditary bullous dystrophy macular type: report of a second family.
Lungarotti MS; Martello C; Barboni G; Mezzetti D; Mariotti G; Calabro A
Am J Med Genet; 1994 Jul; 51(4):598-601. PubMed ID: 7943046
[TBL] [Abstract][Full Text] [Related]
2. Brief clinical report: an X-linked mental retardation syndrome with craniofacial abnormalities, microcephaly and club foot.
Holmes LB; Gang DL
Am J Med Genet; 1984 Jan; 17(1):375-82. PubMed ID: 6711605
[TBL] [Abstract][Full Text] [Related]
3. New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation.
Brooks SS; Wisniewski K; Brown WT
Am J Med Genet; 1994 Jul; 51(4):586-90. PubMed ID: 7943044
[TBL] [Abstract][Full Text] [Related]
4. Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies.
Hamel BC; Mariman EC; van Beersum SE; Schoonbrood-Lenssen AM; Ropers HH
Am J Med Genet; 1994 Jul; 51(4):591-7. PubMed ID: 7943045
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. A new syndrome of dwarfism, brachydactyly, nail dysplasia, and mental retardation in sibs.
Tonoki H; Kishino T; Niikawa N
Am J Med Genet; 1990 May; 36(1):89-93. PubMed ID: 2333912
[TBL] [Abstract][Full Text] [Related]
7. Narrowing the map of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature at Xq12-q21.31.
Shrimpton AE; Braddock BR; Hoo JJ
Am J Med Genet; 2000 May; 92(2):155-6. PubMed ID: 10797443
[No Abstract] [Full Text] [Related]
8. Alopecia, mental retardation, epilepsy and microcephaly in two cousins.
Pridmore C; Baraitser M; Brett EM
Clin Dysmorphol; 1992 Apr; 1(2):79-84. PubMed ID: 1345516
[TBL] [Abstract][Full Text] [Related]
9. Microcephaly and digital anomalies: a newly recognized syndrome of recessively inherited mental retardation.
Kelly TE; Kirson L; Wyatt J
Am J Med Genet; 1993 Feb; 45(3):353-5. PubMed ID: 8434622
[TBL] [Abstract][Full Text] [Related]
10. MEHMO (Mental retardation, Epileptic seizures, Hypogenitalism, Microcephaly, Obesity): a new X-linked mitochondrial disorder.
Leshinsky-Silver E; Zinger A; Bibi CN; Barash V; Sadeh M; Lev D; Sagie TL
Eur J Hum Genet; 2002 Apr; 10(4):226-30. PubMed ID: 12032729
[TBL] [Abstract][Full Text] [Related]
11. A new X-linked syndrome comprising progressive basal ganglion dysfunction, mental and growth retardation, external ophthalmoplegia, postnatal microcephaly and deafness.
Schimke RN; Horton WA; Collins DL; Therou L
Am J Med Genet; 1984 Jan; 17(1):323-32. PubMed ID: 6538752
[TBL] [Abstract][Full Text] [Related]
12. Kabuki syndrome in son and low grade mosaic 45,X/46,XX in mother.
Van Hagen JM; Kwee ML; Madan K; Nieuwint AW; Pals G; ten Kate LP
Genet Couns; 1996; 7(3):201-6. PubMed ID: 8897041
[TBL] [Abstract][Full Text] [Related]
13. [Dubowitz syndrome. A diagnosis not to be missed].
Mathieu M; Berquin P; Epelbaum S; Lenaerts C; Piussan C
Arch Fr Pediatr; 1991 Dec; 48(10):715-8. PubMed ID: 1793348
[TBL] [Abstract][Full Text] [Related]
14. The Borjeson-Forssman-Lehmann syndrome. A family study.
Dereymaeker AM; Fryns JP; Hoefnagels M; Heremans G; Marien J; van den Berghe H
Clin Genet; 1986 Apr; 29(4):317-20. PubMed ID: 3720009
[TBL] [Abstract][Full Text] [Related]
15. Mapping of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature to Xq12-q21.31.
Shrimpton AE; Daly KM; Hoo JJ
Am J Med Genet; 1999 May; 84(3):293-9. PubMed ID: 10331611
[TBL] [Abstract][Full Text] [Related]
16. X-linked syndrome of mental retardation, short stature, and hypertelorism: a new syndrome or a further example of the FG syndrome?
Bottani A
Am J Med Genet; 1994 May; 51(1):87-8. PubMed ID: 8030678
[No Abstract] [Full Text] [Related]
17. X-linked microcephaly, microphthalmia, microcornea, congenital cataract, hypogenitalism, mental deficiency, growth retardation, spasticity: possible new syndrome.
Seemanová E; Lesný I
Am J Med Genet; 1996 Dec; 66(2):179-83. PubMed ID: 8958326
[TBL] [Abstract][Full Text] [Related]
18. A third patient with median cleft upper lip, mental retardation and pugilistic facies (W syndrome): corroboration of a hitherto private syndrome.
Bottani A; Schinzel A
Clin Dysmorphol; 1993 Jul; 2(3):225-31. PubMed ID: 8287184
[TBL] [Abstract][Full Text] [Related]
19. [Cardiac symptoms in 2 patients with Seckel syndrome].
Rappen U; von Brenndorff AI
Monatsschr Kinderheilkd; 1993 Jul; 141(7):584-6. PubMed ID: 8413337
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
