233 related articles for article (PubMed ID: 8074149)
1. Seckel syndrome in a Yemeni family in Saudi Arabia.
Krishna AG; Scrimgeour EM; Zawawi TH
Am J Med Genet; 1994 Jul; 51(3):224-7. PubMed ID: 8074149
[TBL] [Abstract][Full Text] [Related]
2. Studies of microcephalic primordial dwarfism I: approach to a delineation of the Seckel syndrome.
Majewski F; Goecke T
Am J Med Genet; 1982 May; 12(1):7-21. PubMed ID: 7046443
[No Abstract] [Full Text] [Related]
3. An apparently new syndrome of microcephalic primordial dwarfism and cataracts.
Toriello HV; Horton WA; Oostendorp A; Waterman DF; Higgins JV
Am J Med Genet; 1986 Sep; 25(1):1-8. PubMed ID: 3799711
[TBL] [Abstract][Full Text] [Related]
4. Clinical and genetic heterogeneity of Seckel syndrome.
Faivre L; Le Merrer M; Lyonnet S; Plauchu H; Dagoneau N; Campos-Xavier AB; Attia-Sobol J; Verloes A; Munnich A; Cormier-Daire V
Am J Med Genet; 2002 Nov; 112(4):379-83. PubMed ID: 12376940
[TBL] [Abstract][Full Text] [Related]
5. A new locus for Seckel syndrome on chromosome 18p11.31-q11.2.
Børglum AD; Balslev T; Haagerup A; Birkebaek N; Binderup H; Kruse TA; Hertz JM
Eur J Hum Genet; 2001 Oct; 9(10):753-7. PubMed ID: 11781686
[TBL] [Abstract][Full Text] [Related]
6. Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity.
Nakata NM; Guion-Almeida ML; Richieri-Costa A
Am J Med Genet; 1993 Sep; 47(3):330-2. PubMed ID: 8135276
[TBL] [Abstract][Full Text] [Related]
7. Probable autosomal recessive inheritance of polysplenia, situs inversus and cardiac defects in an Amish family.
Arnold GL; Bixler D; Girod D
Am J Med Genet; 1983 Sep; 16(1):35-42. PubMed ID: 6638068
[TBL] [Abstract][Full Text] [Related]
8. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
Bonioli E; Palmieri A; Bertola A; Bellini C
Genet Couns; 1995; 6(4):309-12. PubMed ID: 8775417
[TBL] [Abstract][Full Text] [Related]
9. A case of Seckel syndrome with Tetralogy of Fallot.
Can E; Bulbul A; Uslu S; Demirin H; Comert S; Bolat F; Nuhoglu A
Genet Couns; 2010; 21(1):49-51. PubMed ID: 20420029
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. [OFD syndrome in a male. Clinical-genetic analysis of 33 families].
Segni G; Serra A; Mastrangelo R; Polidori G; Massasso J
Acta Genet Med Gemellol (Roma); 1970 Oct; 19(4):546-66. PubMed ID: 5512530
[No Abstract] [Full Text] [Related]
12. Achalasia and microcephaly.
Dumars KW; Williams JJ; Steele-Sandlin C
Am J Med Genet; 1980; 6(4):309-14. PubMed ID: 7211947
[TBL] [Abstract][Full Text] [Related]
13. A family with three recessive traits and homozygosity for a long 9qh+ chromosome segment.
Christian JC; Dexter RN; Palmer CG; Muller J
Am J Med Genet; 1980; 6(4):301-8. PubMed ID: 6938130
[TBL] [Abstract][Full Text] [Related]
14. Distal aphalangia, syndactyly, and extra metatarsal, associated with short stature, microcephaly, and borderline intelligence: a new autosomal dominant disorder.
Martínez-Frías ML; Martín M; Pardo M; Fernandez de las Heras F; Frías JL
Am J Med Genet; 1995 Jan; 55(2):213-6. PubMed ID: 7717420
[TBL] [Abstract][Full Text] [Related]
15. New syndromes of mental retardation.
Thurmon TF; Santos CL
Birth Defects Orig Artic Ser; 1975; 11(2):264-8. PubMed ID: 1227531
[TBL] [Abstract][Full Text] [Related]
16. Oral-facial-digital syndrome and retinal abnormalities with autosomal recessive inheritance.
Jamieson R; Collins F
Am J Med Genet; 1993 Aug; 47(2):304-6. PubMed ID: 8213926
[No Abstract] [Full Text] [Related]
17. [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]
18. Goldberg-Shprintzen syndrome: Hirschsprung disease, hypotonia, and ptosis in sibs.
Yomo A; Taira T; Kondo I
Am J Med Genet; 1991 Nov; 41(2):188-91. PubMed ID: 1785632
[TBL] [Abstract][Full Text] [Related]
19. Cataract, hypertrichosis, and mental retardation (CAHMR): a new autosomal recessive syndrome.
Temtamy SA; Sinbawy AH
Am J Med Genet; 1991 Dec; 41(4):432-3. PubMed ID: 1776632
[TBL] [Abstract][Full Text] [Related]
20. Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies: a new autosomal recessive syndrome?
Kotzot D; Richter K; Gierth-Fiebig K
Am J Med Genet; 1994 Apr; 50(3):224-7. PubMed ID: 8042664
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
