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Items: 1 to 20 of 133

1.

Retinal dystrophy in the cardiofaciocutaneous syndrome.

Dunya I, Hoon A, Traboulsi EI.

J Pediatr Ophthalmol Strabismus. 1993 Jul-Aug;30(4):264-5. No abstract available.

PMID:
8410580
2.

Cardio-facio-cutaneous (CFC) syndrome: report of two patients without hyperkeratotic skin lesions.

Matsuda Y, Murano I, Kondoh O, Matsuo K, Kajii T.

Am J Med Genet. 1991 May 1;39(2):144-7.

PMID:
1842204
3.

Cardiofaciocutaneous syndrome.

Ades LC, Sillence DO, Rogers M.

Clin Dysmorphol. 1992 Jul;1(3):145-50.

PMID:
1342862
4.

Congenital microcephaly, juvenile retinal dystrophy and normal mentation in a mildly dysmorphic child.

Nguyen TN, Der Kaloustian VM, Barsoum-Homsy M, Dembinska O, Koenekoop RK.

Can J Ophthalmol. 2005 Apr;40(2):195-9. No abstract available.

PMID:
16049536
5.

[Contribution to the differential diagnosis of Smith-Lemli-Opitz syndrome].

Fehlow P.

Padiatr Grenzgeb. 1988;27(4):331-5. German. No abstract available.

PMID:
3174148
6.

Ocular findings in thoracic-pelvic-phalangeal dystrophy.

Allen AW Jr, Moon JB, Hovland KR, Minckler DS.

Arch Ophthalmol. 1979 Mar;97(3):489-92.

PMID:
420637
7.

Holt-Oram syndrome: delayed diagnosis.

Chadha JS, Bayer AJ.

Br J Clin Pract. 1987 May;41(5):754-5. No abstract available.

PMID:
3446267
8.

[A new case of Weaver's syndrome observed in the neonatal period].

Di Comite A, Saracino P, Tonti R, De Vita L.

Pediatria (Napoli). 1983 Oct-Dec;91(4):435-9. Italian. No abstract available.

PMID:
6545407
10.

Tortuosity of the retinal vessels in Aarskog syndrome (faciogenital dysplasia).

Pizio HF, Scott MH, Richard JM.

Ophthalmic Genet. 1994 Mar;15(1):37-40.

PMID:
7953251
11.

Cardio-facio-cutaneous syndrome: report of a case with a review of the literature.

Nanda S, Rajpal M, Reddy BS.

Int J Dermatol. 2004 Jun;43(6):447-50. Review.

PMID:
15186229
12.

Cranioectodermal dysplasia in sibs.

Lang GD, Young ID.

J Med Genet. 1991 Jun;28(6):424. No abstract available.

13.
14.

[Spinocerebellar syndrome of early onset associated with retinal degeneration. Report of a case].

Onsurbe Ramírez I, Lorenzo Sanz G, Aparicio Meix JM.

An Esp Pediatr. 1990 Oct;33(4):387-9. Spanish. No abstract available.

PMID:
2278445
15.

Surgical treatment of the atrial septal aneurysms with concomitant cardiovascular abnormalities.

Ipek G, Mansuroğlu D, Sişmanoglu M, Omeroğlu SN, Mataraci I, Akbayrak H.

Anadolu Kardiyol Derg. 2004 Sep;4(3):266-7. No abstract available.

16.

The Holt Oram syndrome with previously undescribed associated anomalies.

Arora MM, Nath IV, Anand IS, Dhir SP, Sodhi JS, Bidwai PS, Deodhar SD.

J Assoc Physicians India. 1980 Mar-Apr;28(3-4):103-6. No abstract available.

PMID:
7440473
17.

[Fryns syndrome. Report of the first case in Spain].

Rodríguez Gonzalez JT, Echevarría Iturbe C, Lazaro Santander R, García Rojo M, Palacios Calvo J.

An Esp Pediatr. 1990 Apr;32(4):363-4. Spanish. No abstract available.

PMID:
2195944
18.
19.

A new oculorenal syndrome: retinal dystrophy and tubulointerstitial nephropathy in cranioectodermal dysplasia.

Eke T, Woodruff G, Young ID.

Br J Ophthalmol. 1996 May;80(5):490-1. No abstract available.

20.

Ocular manifestations of Seckel syndrome.

Guirgis MF, Lam BL, Howard CW.

Am J Ophthalmol. 2001 Oct;132(4):596-7.

PMID:
11589896
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