118 related articles for article (PubMed ID: 3812569)
1. Dominantly inherited syndrome of microcephaly and congenital lymphedema with normal intelligence.
Leung AK
Am J Med Genet; 1987 Jan; 26(1):231. PubMed ID: 3812569
[No Abstract] [Full Text] [Related]
2. A genetic association between microcephaly and lymphedema.
Meinecke P
Am J Med Genet; 1987 Jan; 26(1):233. PubMed ID: 3812570
[No Abstract] [Full Text] [Related]
3. Total anonychia congenita and microcephaly with normal intelligence: a new autosomal-recessive syndrome?
Teebi AS; Kaurah P
Am J Med Genet; 1996 Dec; 66(3):257-60. PubMed ID: 8985482
[TBL] [Abstract][Full Text] [Related]
4. A genetic association between microcephaly and lymphedema.
Crowe CA; Dickerman LH
Am J Med Genet; 1986 May; 24(1):131-5. PubMed ID: 3706402
[TBL] [Abstract][Full Text] [Related]
5. Dominantly inherited syndrome of microcephaly and congenital lymphedema.
Leung AK
Clin Genet; 1985 Jun; 27(6):611-2. PubMed ID: 4017282
[TBL] [Abstract][Full Text] [Related]
6. Microcephaly/lymphedema and terminal deletion of the long arm of chromosome 13.
Fryns JP
Am J Med Genet; 1995 Jul; 57(3):504. PubMed ID: 7545871
[No Abstract] [Full Text] [Related]
7. Microcephaly, lymphedema, chorioretinopathy and atrial septal defect: a case report and review of the literature.
Eventov-Friedman S; Singer A; Shinwell ES
Acta Paediatr; 2009 Apr; 98(4):758-9. PubMed ID: 19076985
[TBL] [Abstract][Full Text] [Related]
8. Chorioretinal dysplasia-microcephaly-mental retardation syndrome: report of an American family.
Sadler LS; Robinson LK
Am J Med Genet; 1993 Aug; 47(1):65-8. PubMed ID: 8368255
[TBL] [Abstract][Full Text] [Related]
9. Dominantly inherited syndrome of microcephaly and cleft palate.
Halal F
Am J Med Genet; 1983 May; 15(1):135-40. PubMed ID: 6859112
[TBL] [Abstract][Full Text] [Related]
10. [Ophthalmological findings in microcephaly-lymphoedema-chorioretinal dysplasia syndrome].
Hatt Brupbacher SC; Job O; Senn P; Dedes W
Klin Monbl Augenheilkd; 2009 Apr; 226(4):344-6. PubMed ID: 19384796
[TBL] [Abstract][Full Text] [Related]
11. Syndrome of cleft palate, microcephaly, large ears, and short stature (Say syndrome).
Abu-Libdeh B; Fujimoto A; Ehinger M
Am J Med Genet; 1993 Feb; 45(3):358-60. PubMed ID: 8434624
[TBL] [Abstract][Full Text] [Related]
12. Microcephaly, lymphedema, and chorioretinal dysplasia: report of two additional cases.
Angle B; Holgado S; Burton BK; Miller MT; Shapiro MJ; Opitz JM
Am J Med Genet; 1994 Nov; 53(2):99-101. PubMed ID: 7856652
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Autosomal dominant microcephaly--lymphoedema-chorioretinal dysplasia syndrome.
Casteels I; Devriendt K; Van Cleynenbreugel H; Demaerel P; De Tavernier F; Fryns JP
Br J Ophthalmol; 2001 Apr; 85(4):499-500. PubMed ID: 11302131
[No Abstract] [Full Text] [Related]
15. Microcephaly-lymphedema-chorioretinal dysplasia: a unique genetic syndrome with variable expression and possible characteristic facial appearance.
Limwongse C; Wyszynski RE; Dickerman LH; Robin NH
Am J Med Genet; 1999 Sep; 86(3):215-8. PubMed ID: 10482868
[TBL] [Abstract][Full Text] [Related]
16. Microcephaly, lymphedema, and chorioretinal dysplasia: a distinct syndrome?
Feingold M; Bartoshesky L
Am J Med Genet; 1992 Aug; 43(6):1030-1. PubMed ID: 1415329
[TBL] [Abstract][Full Text] [Related]
17. Johanson-Blizzard syndrome with normal intelligence.
Moeschler JB; Lubinsky MS
Am J Med Genet; 1985 Sep; 22(1):69-73. PubMed ID: 4050852
[TBL] [Abstract][Full Text] [Related]
18. Microcephaly, lymphedema, chorioretinal dysplasia (MLCRD) syndrome.
Kelly MN; Khuddus N; Motamarry S; Tuli S
J Pediatr Health Care; 2012; 26(4):306-11. PubMed ID: 22726716
[No Abstract] [Full Text] [Related]
19. Distichiasis-lymphedema. A hereditary syndrome of multiple congenital defects.
Robinow M; Johnson GF; Verhagen AD
Am J Dis Child; 1970 Apr; 119(4):343-7. PubMed ID: 5434594
[No Abstract] [Full Text] [Related]
20. Possible new autosomal recessive syndrome of lymphedema, hydroceles, atrial septal defect, and characteristic facial changes.
Irons MB; Bianchi DW; Geggel RL; Marx GR; Bhan I
Am J Med Genet; 1996 Dec; 66(1):69-71. PubMed ID: 8957515
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]