665 related articles for article (PubMed ID: 8413337)
21. Schinzel-Giedion syndrome. A patient with hypothyroidism and diabetes insipidus.
Santos H; Cordeiro I; Medeira A; Mendonça E; Antunes NL; Rosa FC
Genet Couns; 1994; 5(2):187-9. PubMed ID: 7917131
[TBL] [Abstract][Full Text] [Related]
22. Callosal defect, microcephaly, severe mental retardation, and other anomalies in three sibs.
da-Silva EO
Am J Med Genet; 1988 Apr; 29(4):837-43. PubMed ID: 3400727
[TBL] [Abstract][Full Text] [Related]
23. Trisomy 18 with unilateral atypical ectrodactyly.
Rogers RC
Am J Med Genet; 1994 Jan; 49(1):125-7. PubMed ID: 8172239
[No Abstract] [Full Text] [Related]
24. [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]
25. Association of Duane anomaly with mental retardation, cardiac and urinary tract abnormalities: a new autosomal recessive condition?
Stoll C; Alembik Y; Dott B
Ann Genet; 1994; 37(4):207-9. PubMed ID: 7710257
[TBL] [Abstract][Full Text] [Related]
26. A syndrome of severe midface retraction, multiple skull anomalies, clubfeet, and cardiac and renal malformations in sibs.
Schinzel A; Giedion A
Am J Med Genet; 1978; 1(4):361-75. PubMed ID: 665725
[TBL] [Abstract][Full Text] [Related]
27. [Seckel syndrome. Report of a case].
Colli R; Russo F; Bianchi GA
Minerva Pediatr; 1995 Mar; 47(3):89-91. PubMed ID: 7791718
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. Apparent CHARGE association and chromosome anomaly: chance or contiguous gene syndrome.
Clementi M; Tenconi R; Turolla L; Silvan C; Bortotto L; Artifoni L
Am J Med Genet; 1991 Nov; 41(2):246-50. PubMed ID: 1785643
[TBL] [Abstract][Full Text] [Related]
30. A syndrome of mental retardation, short stature, hemolytic anemia, delayed puberty, and abnormal facial appearance: similarities to a report of aldolase A deficiency.
Hurst JA; Baraitser M; Winter RM
Am J Med Genet; 1987 Dec; 28(4):965-70. PubMed ID: 3688035
[TBL] [Abstract][Full Text] [Related]
31. [Differential diagnostic considerations in microcephalic dwarfism].
Kraft CN; Diedrich O; Wagner U; Schmitt O
Z Orthop Ihre Grenzgeb; 2000; 138(2):126-30. PubMed ID: 10820877
[TBL] [Abstract][Full Text] [Related]
32. Autosomal recessive microcephaly with severe psychomotor retardation.
Scheffer IE; Baraitser M; Wilson J; Godfrey C; Brett EM
Neuropediatrics; 1992 Feb; 23(1):53-6. PubMed ID: 1565220
[TBL] [Abstract][Full Text] [Related]
33. Filippi syndrome: report of three additional cases.
Williams MS; Williams JL; Wargowski DS; Pauli RM; Pletcher BA
Am J Med Genet; 1999 Nov; 87(2):128-33. PubMed ID: 10533026
[TBL] [Abstract][Full Text] [Related]
34. [Russell-Silver syndrome].
Kosaki K; Izumi K; Hasegawa T
Nihon Rinsho; 2006 Sep; Suppl 3():436-9. PubMed ID: 17022582
[No Abstract] [Full Text] [Related]
35. 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]
36. Cardio-facio-cutaneous (CFC) syndrome in a child carrying an inherited inversion of chromosome 7.
Lopez-Rangel E; Hrynchak M; Friedman JM
Am J Med Genet; 1993 Sep; 47(3):326-9. PubMed ID: 8135275
[TBL] [Abstract][Full Text] [Related]
37. Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies.
Elejalde BR; Opitz JM; de Elejalde MM; Gilbert EF; Abellera M; Meisner L; Lebel RR; Hartigan JM
Am J Med Genet; 1984 Apr; 17(4):723-30. PubMed ID: 6539070
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Fountain syndrome: further delineation of the clinical syndrome and follow-up data.
Van Buggenhout GJ; Van Ravenswaaij-Arts CM; Renier WO; Van de Wiel MP; Trommelen JC; Pijkels E; Hamel BC; Fryns JP
Genet Couns; 1996; 7(3):177-86. PubMed ID: 8897038
[TBL] [Abstract][Full Text] [Related]
40. Cerebro-oculo-facio-skeletal (COFS) syndrome. The variability of presenting symptoms as a manifestation of two subtypes?
Casteels I; Wijnants A; Casaer P; Eggermont E; Misotten L; Fryns JP
Genet Couns; 1991; 2(1):43-6. PubMed ID: 1741976
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
