Anton-Lamprecht I - Search Results

1

Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysis.

Zonana J, Schinzel A, Upadhyaya M, Thomas NS, Anton-Lamprecht I, Harper PS. Zonana J, et al. Am J Med Genet. 1990 Jan;35(1):132-5. doi: 10.1002/ajmg.1320350125. Am J Med Genet. 1990. PMID: 2301463

2

Prenatal diagnosis of anhydrotic ectodermal dysplasia.

Anton-Lamprecht I, Arnold ML, Rauskolb R, Schinzel A, Schmid W, Schnyder UW. Anton-Lamprecht I, et al. Hum Genet. 1982;62(2):180. doi: 10.1007/BF00282312. Hum Genet. 1982. PMID: 7160849 No abstract available.

3

Prenatal diagnosis of anhidrotic ectodermal dysplasia.

Arnold ML, Rauskolb R, Anton-Lamprecht I, Schinzel A, Schmid W. Arnold ML, et al. Prenat Diagn. 1984 Mar-Apr;4(2):85-98. doi: 10.1002/pd.1970040202. Prenat Diagn. 1984. PMID: 6739441

4

False-negative prenatal diagnosis of restrictive dermopathy.

Hamel BC, Happle R, Steylen PM, Kollée LA, Stekhoven JH, Nijhuis JG, Rauskolb R, Anton-Lamprecht I. Hamel BC, et al. Am J Med Genet. 1992 Dec 1;44(6):824-6. doi: 10.1002/ajmg.1320440622. Am J Med Genet. 1992. PMID: 1481855

5

Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis.

Dahlqvist J, Klar J, Hausser I, Anton-Lamprecht I, Pigg MH, Gedde-Dahl T Jr, Gånemo A, Vahlquist A, Dahl N. Dahlqvist J, et al. Among authors: anton lamprecht i. J Med Genet. 2007 Oct;44(10):615-20. doi: 10.1136/jmg.2007.050542. Epub 2007 Jun 8. J Med Genet. 2007. PMID: 17557927 Free PMC article.

6

Mutations in the COL5A1 gene are causal in the Ehlers-Danlos syndromes I and II.

De Paepe A, Nuytinck L, Hausser I, Anton-Lamprecht I, Naeyaert JM. De Paepe A, et al. Am J Hum Genet. 1997 Mar;60(3):547-54. Am J Hum Genet. 1997. PMID: 9042913 Free PMC article.

7

[Prenatal diagnosis of genetic dermatoses].

Anton-Lamprecht I, Rauskolb R. Anton-Lamprecht I, et al. Gynakologe. 1994 Oct;27(5):296-308. Gynakologe. 1994. PMID: 7821861 Review. German. No abstract available.

8

Junctional epidermolysis bullosa inversa (locus EBR2A) assigned to 1q31 by linkage and association to LAMC1.

Gedde-Dahl T Jr, Dupuy BM, Jonassen R, Winberg JO, Anton-Lamprecht I, Olaisen B. Gedde-Dahl T Jr, et al. Hum Mol Genet. 1994 Aug;3(8):1387-91. doi: 10.1093/hmg/3.8.1387. Hum Mol Genet. 1994. PMID: 7987320

9

Autosomal recessive anhidrotic ectodermal dysplasia: report of a case and discrimination of diagnostic features.

Anton-Lamprecht I, Schleiermacher E, Wolf M. Anton-Lamprecht I, et al. Birth Defects Orig Artic Ser. 1988;24(2):183-95. Birth Defects Orig Artic Ser. 1988. PMID: 3179426 No abstract available.

10

Problems in prenatal diagnosis of the ichthyosis congenita group.

Arnold ML, Anton-Lamprecht I. Arnold ML, et al. Hum Genet. 1985;71(4):301-11. doi: 10.1007/BF00388455. Hum Genet. 1985. PMID: 4077047

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