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.
111 related articles for article (PubMed ID: 1961207)
21. Infantile lethal variant of Simpson-Golabi-Behmel syndrome associated with hydrops fetalis. Terespolsky D; Farrell SA; Siegel-Bartelt J; Weksberg R Am J Med Genet; 1995 Nov; 59(3):329-33. PubMed ID: 8599356 [TBL] [Abstract][Full Text] [Related]
22. MCA/MR syndrome in two female siblings: new entity or variant examples of Coffin-Lowry versus Atkin-Flaitz syndromes? Jans A; Ippel EF; Dijkstra PF; Bijlsma JB Genet Couns; 1992; 3(3):139-43. PubMed ID: 1388932 [TBL] [Abstract][Full Text] [Related]
23. 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]
24. Ectomorphic habitus, severe mental retardation and characteristic face: a new MCA/MR syndrome? Fryns JP; Smeets E; Thiry P; Geutjens J; Vinken L; Van den Berghe H Am J Med Genet; 1994 Jan; 49(1):91-3. PubMed ID: 8172258 [TBL] [Abstract][Full Text] [Related]
25. New X-linked mental retardation syndrome with the gene mapped tentatively in Xp22.3. Wittwer B; Kircheisen R; Leutelt J; Orth U; Gal A Am J Med Genet; 1996 Jul; 64(1):42-9. PubMed ID: 8826447 [TBL] [Abstract][Full Text] [Related]
26. A new X-linked mental retardation-overgrowth syndrome. Golabi M; Rosen L Am J Med Genet; 1984 Jan; 17(1):345-58. PubMed ID: 6538755 [TBL] [Abstract][Full Text] [Related]
27. Börjeson-Forssman-Lehmann syndrome: further delineation in five cases. Ardinger HH; Hanson JW; Zellweger HU Am J Med Genet; 1984 Dec; 19(4):653-64. PubMed ID: 6517094 [TBL] [Abstract][Full Text] [Related]
28. Genitourinary anomalies of pediatric FG syndrome. Smith JF; Wayment RO; Cartwright PC; Snow BW; Opitz JM J Urol; 2007 Aug; 178(2):656-9. PubMed ID: 17574621 [TBL] [Abstract][Full Text] [Related]
29. [48,XXYY syndrome in a boy with essential tremor. Comparison with 120 cases from the literature]. Donati F; Gasser S; Mullis P; Braga S; Vassella F Monatsschr Kinderheilkd; 1992 Apr; 140(4):216-9. PubMed ID: 1614446 [TBL] [Abstract][Full Text] [Related]
30. Male pseudohermaphroditism with persistent müllerian structures, mental retardation and Borjeson-Forssman-Lehmann-like features: a new syndrome? Verloes A; Gillerot Y; Delfortrie J; Zeevaert-Arnold MT; Collard R; Koulischer L; Fryns JP Genet Couns; 1990; 1(3-4):219-25. PubMed ID: 2098045 [TBL] [Abstract][Full Text] [Related]
31. [X chromosome-linked mental retardation with fragile X chromosome and macro-orchidism]. Zollinger A; Schmid W; Vilan J; Sorg B; Knoblauch M Schweiz Med Wochenschr; 1983 Feb; 113(7):238-44. PubMed ID: 6836249 [TBL] [Abstract][Full Text] [Related]
32. 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]
33. Pentasomy X: report of patient and studies of X-inactivation. Funderburk SJ; Valente M; Klisak I Am J Med Genet; 1981; 8(1):27-33. PubMed ID: 7246603 [TBL] [Abstract][Full Text] [Related]
34. [The 49,XYYYY syndrome: apropos of a case detected at birth and followed for 2 1/2 years]. Plauchu H; Charrin C; Kossmann JC J Genet Hum; 1984 Sep; 32(4):299-306. PubMed ID: 6491641 [TBL] [Abstract][Full Text] [Related]
35. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies. Malpuech G; Demeocq F; Palcoux JB; Vanlieferinghen P Am J Med Genet; 1983 Dec; 16(4):475-80. PubMed ID: 6660246 [TBL] [Abstract][Full Text] [Related]
36. Brief clinical report: renal hypodysplasia and unilateral ovarian agenesis in the penta-X syndrome. Toussi T; Halal F; Lesage R; Delorme F; Bergeron A Am J Med Genet; 1980; 6(2):153-62. PubMed ID: 7446561 [TBL] [Abstract][Full Text] [Related]
37. Kabuki make-up (Niikawa-Kuroki) syndrome with mosaicism ring chromosome X and incomplete XIST gene expression. Su PH; Kuo PL; Chen SJ; Chen JY; Yu JS; Liu YL; Kao IW Acta Paediatr Taiwan; 2007; 48(1):28-31. PubMed ID: 19653414 [TBL] [Abstract][Full Text] [Related]
38. X-linked mental retardation. I. Martin-Bell syndrome (report of 18 families). Rocchi M; Archidiacono N; Filippi G J Genet Hum; 1987 Dec; 35(5):351-79. PubMed ID: 3437265 [TBL] [Abstract][Full Text] [Related]
39. 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]
40. Coexistent mosaic monosomy 21 and fragile X syndrome in a mentally retarded male patient. Utine GE; Aktas D; Boduroğlu K; Alikasifoğlu M; Tunçbilek E Genet Couns; 2007; 18(2):171-7. PubMed ID: 17710869 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]