123 related articles for article (PubMed ID: 225952)
21. The Neu-Laxova syndrome.
Seemanová E; Rudolf R
Am J Med Genet; 1985 Jan; 20(1):13-5. PubMed ID: 3970065
[No Abstract] [Full Text] [Related]
22. Two sibs with microcephaly, hygroma colli, renal dysplasia, and cutaneous syndactyly: a new lethal MCA syndrome?
Janssen HC; Schaap C; Vandevijver N; Moerman P; de Die-Smulders CE; Fryns JP
J Med Genet; 1999 Jun; 36(6):481-4. PubMed ID: 10874639
[TBL] [Abstract][Full Text] [Related]
23. Schinzel-Giedion syndrome: autopsy report and additional clinical manifestations.
Rodríguez JI; Jiménez-Heffernan JA; Leal J
Am J Med Genet; 1994 Dec; 53(4):374-7. PubMed ID: 7864048
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Acrocallosal syndrome in fetus: focus on additional brain abnormalities.
Fernandez C; Soulier M; Coulibaly B; Liprandi A; Benoit B; Giuliano F; Sigaudy S; Figarella-Branger D; Fallet-Bianco C
Acta Neuropathol; 2008 Jan; 115(1):151-6. PubMed ID: 17593378
[TBL] [Abstract][Full Text] [Related]
26. Smith-Lemli-Opitz syndrome-type II: multiple congenital anomalies with male pseudohermaphroditism and frequent early lethality.
Curry CJ; Carey JC; Holland JS; Chopra D; Fineman R; Golabi M; Sherman S; Pagon RA; Allanson J; Shulman S
Am J Med Genet; 1987 Jan; 26(1):45-57. PubMed ID: 3812577
[TBL] [Abstract][Full Text] [Related]
27. [Hair dysplasia in oculo-dento-digital syndrome. Apropos of a mother-daughter case].
Adamski H; Chevrant-Breton J; Odent S; Patoux-Pibouin M; Le Marec B; Laudren A; Urvoy M
Ann Dermatol Venereol; 1994; 121(10):694-9. PubMed ID: 7793757
[TBL] [Abstract][Full Text] [Related]
28. Neu-Laxova syndrome in an appropriate for gestational age newborn.
Dilli D; Yaşar H; Dilmen U; Ceylaner G
Indian J Dermatol Venereol Leprol; 2008; 74(5):487-9. PubMed ID: 19052411
[TBL] [Abstract][Full Text] [Related]
29. Neu-Laxova syndrome: a case report.
Roy S; Begum J; Sharifunnaher B; Saha AK; Afroza S; Islam MZ
Mymensingh Med J; 2014 Jan; 23(1):167-9. PubMed ID: 24584393
[TBL] [Abstract][Full Text] [Related]
30. Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome?
Filippi G
Am J Med Genet; 1985 Dec; 22(4):821-4. PubMed ID: 4073130
[TBL] [Abstract][Full Text] [Related]
31. The Bowen-Conradi syndrome -- a highly lethal autosomal recessive syndrome of microcephaly, micrognathia, low birth weight, and joint deformities.
Hunter AG; Woerner SJ; Montalvo-Hicks LD; Fowlow SB; Haslam RH; Metcalf PJ; Lowry RB
Am J Med Genet; 1979; 3(3):269-79. PubMed ID: 484596
[TBL] [Abstract][Full Text] [Related]
32. Neu-Laxova syndrome: A new patient with detailed antenatal and post-natal findings.
Manar AL; Asma B
Am J Med Genet A; 2010 Dec; 152A(12):3193-6. PubMed ID: 21108408
[No Abstract] [Full Text] [Related]
33. Craniodigital syndromes: report of a child with Filippi syndrome and discussion of differential diagnosis.
Toriello HV; Higgins JV
Am J Med Genet; 1995 Jan; 55(2):200-4. PubMed ID: 7717418
[TBL] [Abstract][Full Text] [Related]
34. Neu-Laxova syndrome: report of a case from Turkey.
Kuseyri F; Bilge I; Bilgiç L; Apak MY
Clin Genet; 1993 May; 43(5):267-9. PubMed ID: 8375108
[TBL] [Abstract][Full Text] [Related]
35. A spectrum of phenotypical expression OF Neu-Laxova syndrome: Three case reports and a review of the literature.
Coto-Puckett WL; Gilbert-Barness E; Steelman CK; Stuart T; Robinson HB; Shehata BM
Fetal Pediatr Pathol; 2010 Jan; 29(2):108-19. PubMed ID: 20334486
[TBL] [Abstract][Full Text] [Related]
36. Sclerocornea, hypertelorism, syndactyly, and ambiguous genitalia.
Martínez-Frías ML; Bermejo E; Sánchez Otero T; Urioste M; Morena V; Cruz E
Am J Med Genet; 1994 Jan; 49(2):195-7. PubMed ID: 8116666
[TBL] [Abstract][Full Text] [Related]
37. Bartsocas-Papas syndrome in an Arab family with four affected sibs: further characterization.
Massoud AA; Ammaari AN; Khan AS; ven Katraman B; Teebi AS
Am J Med Genet; 1998 Aug; 79(1):16-21. PubMed ID: 9738862
[TBL] [Abstract][Full Text] [Related]
38. Prenatal diagnosis of Neu-Laxova syndrome: a case report.
Aslan H; Gul A; Polat I; Mutaf C; Agar M; Ceylan Y
BMC Pregnancy Childbirth; 2002; 2(1):1. PubMed ID: 11895570
[TBL] [Abstract][Full Text] [Related]
39. Prenatal sonographic diagnosis of Neu-Laxova syndrome.
Durr-e-Sabih ; Khan AN; Sabih Z
J Clin Ultrasound; 2001; 29(9):531-4. PubMed ID: 11745866
[TBL] [Abstract][Full Text] [Related]
40. New manifestations in an infant with Neu Laxova syndrome.
Rouzbahani L
Am J Med Genet; 1995 Mar; 56(2):239-40. PubMed ID: 7625453
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
