Lacombe D - Search Results

1

Contribution of PTEN large rearrangements in Cowden disease: a multiplex amplifiable probe hybridisation (MAPH) screening approach.

Chibon F, Primois C, Bressieux JM, Lacombe D, Lok C, Mauriac L, Taieb A, Longy M. Chibon F, et al. Among authors: lacombe d. J Med Genet. 2008 Oct;45(10):657-65. doi: 10.1136/jmg.2008.058131. Epub 2008 May 2. J Med Genet. 2008. PMID: 18456716

2

New case of Toriello-Carey syndrome.

Lacombe D, Creusot G, Battin J. Lacombe D, et al. Am J Med Genet. 1992 Feb 1;42(3):374-6. doi: 10.1002/ajmg.1320420325. Am J Med Genet. 1992. PMID: 1536182

3

Proteus syndrome in 7 patients: clinical and genetic considerations.

Lacombe D, Taieb A, Vergnes P, Sarlangue J, Chateil JF, Bucco P, Nelson JR, Battin J, Maleville J. Lacombe D, et al. Genet Couns. 1991;2(2):93-101. Genet Couns. 1991. PMID: 1781960

4

Neonatal Noonan syndrome with a molluscoid cutaneous excess over the scalp.

Lacombe D, Taieb A, Masson P, Fayon M, Demarquez JL. Lacombe D, et al. Genet Couns. 1991;2(4):249-53. Genet Couns. 1991. PMID: 1799426

5

The gene for Bazex-Dupré-Christol syndrome maps to chromosome Xq.

Vabres P, Lacombe D, Rabinowitz LG, Aubert G, Anderson CE, Taieb A, Bonafé JL, Hors-Cayla MC. Vabres P, et al. Among authors: lacombe d. J Invest Dermatol. 1995 Jul;105(1):87-91. doi: 10.1111/1523-1747.ep12313359. J Invest Dermatol. 1995. PMID: 7615983 Free article.

6

Overlap between the Bazex syndrome and congenital hypotrichosis and milia.

Lacombe D, Taïeb A. Lacombe D, et al. Am J Med Genet. 1995 May 8;56(4):423-4. doi: 10.1002/ajmg.1320560415. Am J Med Genet. 1995. PMID: 7677860 No abstract available.

7

[Erythromelalgia: a familial case. Discussion on the role of mercury].

Martin JC, Lacombe D, Lefebvre D, Bonafé JL, Taïeb A, Maleville J. Martin JC, et al. Among authors: lacombe d. Ann Dermatol Venereol. 1994;121(4):309-14. Ann Dermatol Venereol. 1994. PMID: 7702249 French.

8

Congenital hypotrichosis and milia: report of a large family suggesting X-linked dominant inheritance.

Rapelanoro R, Taïeb A, Lacombe D. Rapelanoro R, et al. Among authors: lacombe d. Am J Med Genet. 1994 Oct 1;52(4):487-90. doi: 10.1002/ajmg.1320520417. Am J Med Genet. 1994. PMID: 7747764

9

[Unusual form of Noonan syndrome: neonatal multi-organ involvement with chylothorax and nevoid Cutis verticis gyrata].

Masson P, Fayon M, Lamireau T, Llanas B, Lacombe D, Taïeb A, Demarquez JL. Masson P, et al. Among authors: lacombe d. Pediatrie. 1993;48(1):59-62. Pediatrie. 1993. PMID: 8392694 French.

10

Split hand/split foot deformity and LADD syndrome in a family: overlap between the EEC and LADD syndromes.

Lacombe D, Serville F, Marchand D, Battin J. Lacombe D, et al. J Med Genet. 1993 Aug;30(8):700-3. doi: 10.1136/jmg.30.8.700. J Med Genet. 1993. PMID: 8411061 Free PMC article.

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