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Items: 1 to 20 of 101

1.

A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies.

Cohen MM Jr, Hall BD, Smith DW, Graham CB, Lampert KJ.

J Pediatr. 1973 Aug;83(2):280-4. No abstract available.

PMID:
4717588
2.

[Cohen syndrome in 2 brothers].

Zetler S, Römke C, Aksu F.

Klin Padiatr. 1987 Jan-Feb;199(1):55-7. German.

PMID:
3560767
3.
4.

Cohen syndrome.

Alavi S, Kher A, Kumar A, Muranjan M, Bharucha B.

Indian Pediatr. 1993 May;30(5):678-81. No abstract available.

PMID:
8282400
5.

Diaphragmatic defects, craniofacial dysmorphism, cleft palate and distal limb deformities. - a new lethal syndrome.

Goddeeris P, Fryns JP, van den Berghe H.

J Genet Hum. 1980 Mar;28(1):57-60.

PMID:
7400786
6.

Acrofacial dysostosis with postaxial limb deficiency.

Fryns JP, Van den Berghe H.

Am J Med Genet. 1988 Jan;29(1):205-8.

PMID:
3344768
7.

The Velo-Cardio-Facial (Shprintzen) syndrome.

Johnson CD, Ceino Sena CM.

Bol Asoc Med P R. 1990 Jan;82(1):25-7. No abstract available.

PMID:
2317247
8.

Marshall-Smith syndrome: new aspects.

Roodhooft AM, Van Acker KJ, Van Thienen MN, Martin JJ, Ceuterick C.

Neuropediatrics. 1988 Nov;19(4):179-82.

PMID:
3205374
9.

[Cohen's syndrome in 2 sisters].

Doyard P, Mattei JF.

Sem Hop. 1984 Apr 12;60(16):1143-7. French.

PMID:
6326307
10.

FG syndrome: the trias mental retardation, hypotonia and constipation reviewed.

Zwamborn-Hanssen AM, Schrander-Stumpel CT, Smeets E, Decock P, Fryns JP.

Genet Couns. 1995;6(4):313-9.

PMID:
8775418
11.

An oculocerebrofacial syndrome.

Kaufman RL, Rimoin DL, Prensky AL, Sly WS.

Birth Defects Orig Artic Ser. 1971 Feb;7(1):135-8.

PMID:
5006210
12.

Cardiac involvement in the Cohen syndrome: a case report.

Sack J, Friedman E.

Clin Genet. 1980 May;17(5):317-9.

PMID:
7438489
13.

[Pena-Shokeir syndrome: report of a case with benign outcome].

Romeo MG, Betta P, Rodonò A, Tina LG, Distefano G.

Pediatr Med Chir. 1995 Jan-Feb;17(1):73-5. Italian.

PMID:
7739933
14.

[Touraine's centrofacial lentiginosis (CFL)].

Dociu I, Galaction-Niţelea O, Sírjiţă N, Murgu V.

Neurol Psihiatr Neurochir. 1974 Jan-Feb;19(1):21-6. Romanian. No abstract available.

PMID:
4596188
15.
16.
17.

Lujan-Fryns syndrome (X-linked mental retardation with marfanoid habitus): report of three cases and review.

Lacombe D, Bonneau D, Verloes A, Couet D, Koulischer L, Battin J.

Genet Couns. 1993;4(3):193-8.

PMID:
8267926
18.

The Cohen syndrome.

Fryns JP, Van den Berghe H.

J Genet Hum. 1981 Dec;29(4):449-53.

PMID:
7328419
19.

Craniofrontonasal dysplasia.

Young ID.

J Med Genet. 1987 Apr;24(4):193-6. No abstract available.

20.

Microcephaly, distinctive facies, single atrium, postaxial polydactyly, skeletal defects and mental retardation: a new familial faciocardiomelic syndrome?

García-Ortiz JE, García-Cruz D, Dávalos IP, Nazará Z, García-Cruz MO, Castañeda V, Gutiérrez-Mendivil L, Sánchez-Corona J.

Clin Dysmorphol. 2007 Jan;16(1):15-20.

PMID:
17159509

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