Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 18

1.

Brachydactyly type B1: report of a family with de novo ROR2 mutation.

Hamamy H, Saleh N, Oldridge M, Al-Hadidy A, Ajlouni K.

Clin Genet. 2006 Dec;70(6):538-40. No abstract available.

PMID:
17101003
2.

Human HOX gene mutations.

Goodman FR, Scambler PJ.

Clin Genet. 2001 Jan;59(1):1-11. Review.

PMID:
11206481
3.

Ectrodactyly-mandibulo-facial dysostosis: case report and delineation of an entity.

Turnpenny PD, Johnston AW, Dean JC, Haites NE, Couzin DA, Stephen GS.

Clin Dysmorphol. 1992 Apr;1(2):103-9. Review.

PMID:
1345512
4.

Cooks syndrome: a case report and brief review.

Brennan CB, Buehler T, Lesher JL Jr.

Pediatr Dermatol. 2013 Jul-Aug;30(4):e52-3. doi: 10.1111/j.1525-1470.2011.01668.x. Review.

PMID:
22329539
5.

Greig cephalopolysyndactyly syndrome in a large family: a comparison of the clinical signs with those described in the literature.

Ausems MG, Ippel PF, Renardel de Lavalette PA.

Clin Dysmorphol. 1994 Jan;3(1):21-30. Review.

PMID:
8205322
6.

Robinow syndrome.

Patton MA, Afzal AR.

J Med Genet. 2002 May;39(5):305-10. Review.

7.

The pattern of shortened hand and foot bones in D- and E-brachydactyly and pseudohypoparathyroidism/pseudopseudohypoparathyroidism.

Graudal N, Galløe A, Christensen H, Olesen K.

Rofo. 1988 Apr;148(4):460-2. Review. No abstract available.

PMID:
2834801
8.

The expanding panorama of split hand foot malformation.

Basel D, Kilpatrick MW, Tsipouras P.

Am J Med Genet A. 2006 Jul 1;140(13):1359-65. Review.

PMID:
16763964
9.

Central ray deficiency with extensive syndactyly: a dilemma for classification.

Elliott AM, Reed MH, Evans JA.

Genet Couns. 2009;20(1):27-43. Review.

PMID:
19400540
10.

Split hand foot malformation (SHFM).

Elliott AM, Evans JA, Chudley AE.

Clin Genet. 2005 Dec;68(6):501-5. Review.

PMID:
16283879
11.

Cenani-Lenz syndrome: report of a new case and review of the literature.

Nezarati MM, McLeod DR.

Clin Dysmorphol. 2002 Jul;11(3):215-8. Review.

PMID:
12072805
12.

Keipert syndrome: two further cases and review of the literature.

Nik-Zainal S, Holder SE, Cruwys M, Hall CM, Shaw-Smith C.

Clin Dysmorphol. 2008 Jul;17(3):169-75. doi: 10.1097/MCD.0b013e3282f4afc3. Review. No abstract available.

PMID:
18541962
13.

Waardenburg anophthalmia syndrome: report and review.

Cogulu O, Ozkinay F, Gündüz C, Sapmaz G, Ozkinay C.

Am J Med Genet. 2000 Jan 17;90(2):173-4. Review. No abstract available.

PMID:
10607960
14.

Answering a century old riddle: brachydactyly type A1.

Gao B, He L.

Cell Res. 2004 Jun;14(3):179-87. Review.

15.

A novel syndrome with psychiatric features and review of malformation syndromes with psychiatric disorders.

du Souich C, Austin JC, Friedlander R, Boerkoel CF.

Am J Med Genet A. 2009 Feb 15;149A(4):713-21. doi: 10.1002/ajmg.a.32709. Review.

PMID:
19253384
16.

Symmetrical absence of hands and feet with bilateral radius agenesia: case report of a new entity?

Machado Rosa RF, Gazzola Zen PR, Machado Neto L, Graziadio C, Paskulin GA.

Clin Dysmorphol. 2006 Oct;15(4):235-7. Review. No abstract available.

PMID:
16957481
17.

[Hand-foot-genital syndrome].

Ieshima A.

Ryoikibetsu Shokogun Shirizu. 2001;(33):785-6. Review. Japanese. No abstract available.

PMID:
11462685
18.

[Acheiropody].

Matsuo M.

Ryoikibetsu Shokogun Shirizu. 2001;(33):89. Review. Japanese. No abstract available.

PMID:
11462731
Items per page

Supplemental Content

Support Center