Lacombe D - Search Results

1

18p monosomy with midline defects and a de novo satellite identified by FISH.

Taine L, Goizet C, Wen ZQ, Chateil JF, Battin J, Saura R, Lacombe D. Taine L, et al. Among authors: lacombe d. Ann Genet. 1997;40(3):158-63. Ann Genet. 1997. PMID: 9401105

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

Floating-Harbor syndrome: description of a further patient, review of the literature, and suggestion of autosomal dominant inheritance.

Lacombe D, Patton MA, Elleau C, Battin J. Lacombe D, et al. Eur J Pediatr. 1995 Aug;154(8):658-61. doi: 10.1007/BF02079072. Eur J Pediatr. 1995. PMID: 7588969 Review.

7

[Dysmorphology and syndromes: a job for genetic and pediatric specialists].

Battin J, Lacombe D. Battin J, et al. Among authors: lacombe d. Arch Pediatr. 1995 Jul;2(7):615-8. doi: 10.1016/0929-693x(96)81213-9. Arch Pediatr. 1995. PMID: 7663647 Review. French. No abstract available.

8

Clinical identification of a human equivalent to the short ear (se) murine phenotype.

Lacombe D, Toutain A, Gorlin RJ, Oley CA, Battin J. Lacombe D, et al. Ann Genet. 1994;37(4):184-91. Ann Genet. 1994. PMID: 7710253

9

Congenital marked hypertrichosis and Laband syndrome in a child: overlap between the gingival fibromatosis-hypertrichosis and Laband syndromes.

Lacombe D, Bioulac-Sage P, Sibout M, Daussac E, Lesure F, Manchart JP, Battin J. Lacombe D, et al. Genet Couns. 1994;5(3):251-6. Genet Couns. 1994. PMID: 7811425

10

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.

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