Similar articles for PMID: 10213037

Year	Number of Results
1971	1
1972	3
1973	4
1974	6
1975	3
1976	3
1977	2
1978	2
1979	5
1980	2
1981	1
1982	3
1983	3
1984	6
1985	5
1986	1
1987	3
1988	1
1989	6
1991	2
1992	4
1993	4
1994	2
1995	1
1996	2
1997	5
1998	4
1999	2
2000	5
2001	3
2002	4
2003	1
2004	2
2005	2
2006	2
2007	2
2008	1
2009	2
2011	1
2012	1
2013	1
2015	3
2016	1
2017	2
2018	2
2019	1
2020	1
2021	1
2022	1
2024	0

1

Robinow (fetal face) syndrome: report of a boy with dominant type and an infant with recessive type.

Kantaputra PN, Gorlin RJ, Ukarapol N, Unachak K, Sudasna J. Kantaputra PN, et al. Am J Med Genet. 1999 May 7;84(1):1-7. doi: 10.1002/(sici)1096-8628(19990507)84:1<1::aid-ajmg1>3.0.co;2-c. Am J Med Genet. 1999. PMID: 10213037

2

Craniofacial dysostosis, hypertrichosis, genital hypoplasia, ocular, dental, and digital defects: confirmation of the Gorlin-Chaudhry-Moss syndrome.

Ippel PF, Gorlin RJ, Lenz W, van Doorne JM, Bijlsma JB. Ippel PF, et al. Am J Med Genet. 1992 Nov 1;44(4):518-22. doi: 10.1002/ajmg.1320440428. Am J Med Genet. 1992. PMID: 1442899

3

Autosomal recessive acro-fronto-facio-nasal dysostosis associated with genitourinary anomalies: a third case report.

Chaabouni M, Maazoul F, Ben Hamida A, Berhouma M, Marrakchi Z, Chaabouni H. Chaabouni M, et al. Am J Med Genet A. 2008 Jul 15;146A(14):1825-7. doi: 10.1002/ajmg.a.32349. Am J Med Genet A. 2008. PMID: 18553510

4

[Feingold syndrome].

Alessandri JL, Graber D, Tiran-Rajaofera I, Montbrun A, Pilorget H, Samperiz S, Attali T, de Napoli-Cocci S. Alessandri JL, et al. Arch Pediatr. 2000 Jun;7(6):637-40. doi: 10.1016/s0929-693x(00)80132-3. Arch Pediatr. 2000. PMID: 10911531 French.

5

A particular form of cranio-facio-mandibular dysostosis with type B brachydactylia.

Van Damme W, Touitou D. Van Damme W, et al. J Belge Radiol. 1980;63(4):491-6. J Belge Radiol. 1980. PMID: 7204325 No abstract available.

6

Familial polysyndactyly and craniofacial anomalies.

Hootnick D, Holmes LB. Hootnick D, et al. Clin Genet. 1972;3(2):128-34. doi: 10.1111/j.1399-0004.1972.tb01734.x. Clin Genet. 1972. PMID: 4340995 No abstract available.

7

The Greig cephalopolysyndactyly syndrome in a Canadian family.

Chudley AE, Houston CS. Chudley AE, et al. Am J Med Genet. 1982 Nov;13(3):269-76. doi: 10.1002/ajmg.1320130307. Am J Med Genet. 1982. PMID: 6295159 No abstract available.

8

Robin sequence and oligodactyly in mother and son--probably a further example of the postaxial acrofacial dysostosis syndrome.

Meinecke P, Wiedemann HR. Meinecke P, et al. Am J Med Genet. 1987 Aug;27(4):953-7. doi: 10.1002/ajmg.1320270423. Am J Med Genet. 1987. PMID: 3425604 No abstract available.

9

The Coffin-Siris syndrome.

Schinzel A. Schinzel A. Acta Paediatr Scand. 1979 May;68(3):449-52. doi: 10.1111/j.1651-2227.1979.tb05037.x. Acta Paediatr Scand. 1979. PMID: 155976

10

Postaxial acrofacial dysostosis syndrome.

Miller M, Fineman R, Smith DW. Miller M, et al. J Pediatr. 1979 Dec;95(6):970-5. doi: 10.1016/s0022-3476(79)80285-1. J Pediatr. 1979. PMID: 501501

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

124 results

Results by year