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Results: 1 to 20 of 119

Similar articles for PubMed (Select 1642273)

1.

New mental retardation syndrome with hearing impairment, distinct facial appearance, and skeletal anomalies.

Finucane B, Kurtz MB, Scott CI Jr.

Am J Med Genet. 1992 Jul 15;43(5):844-7.

PMID:
1642273
2.

KBG syndrome in a cohort of Italian patients.

Brancati F, D'Avanzo MG, Digilio MC, Sarkozy A, Biondi M, De Brasi D, Mingarelli R, Dallapiccola B.

Am J Med Genet A. 2004 Dec 1;131(2):144-9.

PMID:
15523620
5.

New multiple congenital anomalies: mental retardation syndrome (MCA/MR) with facio-cutaneous-skeletal involvement.

Borochowitz Z, Pavone L, Mazor G, Rizzo R, Dar H.

Am J Med Genet. 1992 Jul 1;43(4):678-85. Review.

PMID:
1621757
6.

Further delineation of the KBG syndrome.

Devriendt K, Holvoet M, Fryns JP.

Genet Couns. 1998;9(3):191-4.

PMID:
9777340
7.
8.
9.

Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation.

Hennekam RC, Geerdink RA, Hamel BC, Hennekam FA, Kraus P, Rammeloo JA, Tillemans AA.

Am J Med Genet. 1989 Dec;34(4):593-600.

PMID:
2624276
10.

[Smith-Magenis syndrome].

Lacombe D, Moncla A, Malzac P, Mattei MG, Battin J.

Arch Pediatr. 1997 May;4(5):438-42. French.

PMID:
9230994
11.

Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndrome.

Chen H, Immken L, Lachman R, Yang S, Rimoin DL, Rightmire D, Eteson D, Stewart F, Beemer FA, Opitz JM, et al.

Am J Med Genet. 1984 Apr;17(4):809-26.

PMID:
6720746
14.

The KBG syndrome-a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomalies.

Herrmann J, Pallister PD, Tiddy W, Opitz JM.

Birth Defects Orig Artic Ser. 1975;11(5):7-18. No abstract available.

PMID:
1218237
15.

A second patient with Tsukahara syndrome: type A1 brachydactyly, short stature, hearing loss, microcephaly, mental retardation and ptosis.

Utine GE, Breckpot J, Thienpont B, Alanay Y, Aksoy C, Boduroğlu K, Devriendt K.

Am J Med Genet A. 2010 Apr;152A(4):947-9. doi: 10.1002/ajmg.a.33325.

PMID:
20358606
16.

Microcephaly, macrotia, unusual mimics and mental retardation syndrome: new syndrome or variant of De Lange type 2 syndrome.

Verloes A, Lesenfants S, Philippet B, Iyawa A, Laloux F, Koulischer L.

Genet Couns. 1996;7(4):277-82.

PMID:
8985731
17.

A new X-linked mental retardation syndrome.

Atkin JF, Flaitz K, Patil S, Smith W.

Am J Med Genet. 1985 Aug;21(4):697-705.

PMID:
4025397
18.

Apparent Ruvalcaba syndrome with genitourinary abnormalities.

Bialer MG, Wilson WG, Kelly TE.

Am J Med Genet. 1989 Jul;33(3):314-7. Review.

PMID:
2679089
19.

The Dubowitz syndrome.

Küster W, Majewski F.

Eur J Pediatr. 1986 Apr;144(6):574-8.

PMID:
3709570
20.
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