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Items: 1 to 20 of 23

1.
2.

Genitopatellar syndrome, sensorineural hearing loss, and cleft palate.

Bergmann C, Spranger S, Javaher P, Ptok M.

Oral Maxillofac Surg. 2011 Jun;15(2):103-6. doi: 10.1007/s10006-009-0202-4. Review.

PMID:
20182757
3.

Meier-Gorlin syndrome: report of eight additional cases and review.

Bongers EM, Opitz JM, Fryer A, Sarda P, Hennekam RC, Hall BD, Superneau DW, Harbison M, Poss A, van Bokhoven H, Hamel BC, Knoers NV.

Am J Med Genet. 2001 Aug 1;102(2):115-24. Review.

PMID:
11477602
4.

Differential diagnosis on the basis of physical findings.

Hanshaw JB, Dudgeon JA.

Major Probl Clin Pediatr. 1978;17:278-300. Review. No abstract available.

PMID:
340801
5.

Meier-Gorlin syndrome.

de Munnik SA, Hoefsloot EH, Roukema J, Schoots J, Knoers NV, Brunner HG, Jackson AP, Bongers EM.

Orphanet J Rare Dis. 2015 Sep 17;10:114. doi: 10.1186/s13023-015-0322-x. Review.

6.

Additional case of Tsukahara's syndrome or new syndrome: further delineation of the association of microcephaly and radio-ulnar synostosis.

Selicorni A, Ferrarini A, Cagnoli G, Fratoni A, Bottigelli M, Milani D.

Am J Med Genet A. 2005 Jan 15;132A(2):189-90. Review.

PMID:
15578583
7.

Mental deficiency, alterations in performance, and CNS abnormalities in overgrowth syndromes.

Cohen MM Jr.

Am J Med Genet C Semin Med Genet. 2003 Feb 15;117C(1):49-56. Review.

PMID:
12561058
8.

Further arguments for non-fortuitous association of Potter sequence with XYY males.

Rudnik-Schöneborn S, Schüler HM, Schwanitz G, Hansmann M, Zerres K.

Ann Genet. 1996;39(1):43-6. Review.

PMID:
9297443
9.

[Schinzel-Giedion syndrome].

Okamoto N.

Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):35-7. Review. Japanese. No abstract available.

PMID:
11057134
10.

Filippi syndrome: further clinical characterization.

Battaglia A, Filippi T, Pusceddu S, Williams CA.

Am J Med Genet A. 2008 Jul 15;146A(14):1848-52. doi: 10.1002/ajmg.a.32400. Review.

PMID:
18553552
11.

Hearing impairment, undescended testis, circumferential skin creases, and mental handicap (HITCH) syndrome: a case report.

Kondoh T, Eguchi J, Hamasaki Y, Doi T, Kinoshita E, Matsumoto T, Abe K, Ohtani Y, Moriuchi H.

Am J Med Genet A. 2004 Mar 15;125A(3):290-2. Review.

PMID:
14994239
12.

Malpuech syndrome: three patients and a review.

Kerstjens-Frederikse WS, Brunner HG, van Dael CM, van Essen AJ.

Am J Med Genet A. 2005 May 1;134(4):450-3. Review.

PMID:
15793834
13.

Microcephaly is not mandatory for the diagnosis of mosaic variegated aneuploidy syndrome.

Callier P, Faivre L, Cusin V, Marle N, Thauvin-Robinet C, Sandre D, Rousseau T, Sagot P, Lacombe E, Faber V, Mugneret F.

Am J Med Genet A. 2005 Aug 30;137(2):204-7. Review.

PMID:
16059936
14.

[Trisomy 22. A new case].

Berger R, Lejeune C, de Paillerets F.

Ann Pediatr (Paris). 1976 Nov 2;23(11):705-11. Review. French. No abstract available.

PMID:
16106879
15.

MICRO syndrome: an entity distinct from COFS syndrome.

Graham JM Jr, Hennekam R, Dobyns WB, Roeder E, Busch D.

Am J Med Genet A. 2004 Jul 30;128A(3):235-45. Review.

PMID:
15216543
16.

Urorectal septum malformation sequence: prenatal progression, clinical report, and embryology review.

Escobar LF, Heiman M, Zimmer D, Careskey H.

Am J Med Genet A. 2007 Nov 15;143A(22):2722-6. Review.

PMID:
17937427
17.

Index of suspicion.

[No authors listed]

Pediatr Rev. 2003 Apr;24(4):137-42. Review. No abstract available. Erratum in: Pediatr Rev. 2003/24(9):319.

PMID:
12671100
18.
19.

[Tonoki syndrome].

Tonoki H.

Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):734-5. Review. Japanese. No abstract available.

PMID:
11528994
20.

[Martsolf syndrome].

Izumikawa Y.

Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):149. Review. Japanese. No abstract available.

PMID:
11528667
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