Lacombe D - Search Results

1

Association of external auditory canal atresia, vertical talus, and hypertelorism: confirmation of Rasmussen syndrome.

Julia S, Pedespan JM, Boudard P, Barbier R, Gavilan-Cellie I, Chateil JF, Lacombe D. Julia S, et al. Among authors: lacombe d. Am J Med Genet. 2002 Jun 15;110(2):179-81. doi: 10.1002/ajmg.10433. Am J Med Genet. 2002. PMID: 12116258

2

Confirmation of assignment of a locus for Rubinstein-Taybi syndrome gene to 16p13.3.

Lacombe D, Saura R, Taine L, Battin J. Lacombe D, et al. Am J Med Genet. 1992 Sep 1;44(1):126-8. doi: 10.1002/ajmg.1320440134. Am J Med Genet. 1992. PMID: 1519642

3

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

4

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

5

Medulloblastoma in the nevoid basal-cell carcinoma syndrome: case reports and review of the literature.

Lacombe D, Chateil JF, Fontan D, Battin J. Lacombe D, et al. Genet Couns. 1990;1(3-4):273-7. Genet Couns. 1990. PMID: 2098052 Review.

6

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

7

Severe presentation of Peters'-Plus syndrome.

Lacombe D, Llanas B, Chateil JF, Sarrazin E, Carles D, Battin J. Lacombe D, et al. Clin Dysmorphol. 1994 Oct;3(4):358-60. Clin Dysmorphol. 1994. PMID: 7894743 No abstract available.

8

[Coffin-Lowry syndrome and hyperprolinemia].

Lacombe D, Parrot-Roulaud F, Castell JF, Serville F, Hehunstre JP, Battin J. Lacombe D, et al. Arch Fr Pediatr. 1993 Jun-Jul;50(6):489-92. Arch Fr Pediatr. 1993. PMID: 8135609 French.

9

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.

10

Familial occurrence of hereditary renal adysplasia with müllerian anomalies.

Battin J, Lacombe D, Leng JJ. Battin J, et al. Among authors: lacombe d. Clin Genet. 1993 Jan;43(1):23-4. doi: 10.1111/j.1399-0004.1993.tb04420.x. Clin Genet. 1993. PMID: 8462192

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