J. Battin

发表

Altered sensitivity to colchicine and PHA in human cultured cells

Y. Chamla, M. Roumy, M. Lassègues, 1980, Human Genetics.

Study of final height in Turner's syndrome: ethnic and genetic influences.

C. Sultan, J. Limal, G. Simonin, 1994, Acta paediatrica.

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

D. Lacombe, D. Marchand, J. Battin, 1993, Journal of medical genetics.

X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 gene

D. Pham‐Dinh, P. Latour, F. Sturtz, 1996, Human Genetics.

Marfanoid features and craniosynostosis: report of one case and review

D. Lacombe, J. Battin, 1993, Clinical dysmorphology.

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

D. Lacombe, J. Chateil, D. Fontan, 1990, Genetic counseling.

Actualitédu syndrome de Turner

J. Battin, 1996 .

Lujan-Fryns syndrome (X-linked mental retardation with marfanoid habitus): report of three cases and review.

L. Koulischer, A. Verloes, D. Lacombe, 1993, Genetic counseling.

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

D. Lacombe, L. Taine, R. Saura, 1992, American journal of medical genetics.

Familial occurrence of hereditary renal adysplasia with Müllerian anomalies

D. Lacombe, J. Leng, J. Battin, 1993, Clinical Genetics.

Syndrome de Smith-Magenis

M. Mattei, D. Lacombe, A. Moncla, 1997 .

New case of Toriello-Carey syndrome.

D. Lacombe, J. Battin, G. Creusot, 1992, American journal of medical genetics.

Final height in Turner syndrome patients treated with growth hormone.

P. Czernichow, Y. Le Bouc, P. Chatelain, 1995, Hormone research.

Germinal mosaicism in oculo-auriculo-vertebral dysplasia?

D. Lacombe, J. Battin, 1993, American journal of medical genetics.

Partial 9q trisomy associated with a 9,21 translocation

Y. Chamla, J. Battin, M. Micheau, 1977, Human Genetics.

Infantile acute hemorrhagic edema of the skin: study of ten cases.

A. Taïeb, J. Maleville, J. M. Guillard, 1991, Journal of the American Academy of Dermatology.

Betaxolol and propranolol in glucagon stimulation of growth hormone.

J. Coquelin, M. Colle, P. Rochiccioli, 1984, Archives of Disease in Childhood.

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

D. Lacombe, L. Taine, C. Goizet, 1997, Annales de genetique.

Isolated macrodactyly and Proteus syndrome.

D. Lacombe, J. Battin, 1996, Clinical dysmorphology.

[Precocious puberty in children adopted from foreign countries].

J. Limal, A. David, S. Baron, 2000, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

[De novo del (13) (q31.1----qter) in a girl. Effect of gene dosage on blood coagulation factors VII and X].

J. Battin, F. Serville, M. Mullon, 1988, Journal de genetique humaine.

Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counselling

D. Lacombe, C. Yardin, S. Briault, 2002, Prenatal diagnosis.

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

P. Bioulac-Sage, D. Lacombe, F. Lesure, 1994, Genetic counseling.

Pseudoscleroderma and Phenylketonuria

J. Maleville, G. Guillet, N. Doré, 1983, International Journal of Dermatology.

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

M. Patton, D. Lacombe, C. Elleau, 1995, European Journal of Pediatrics.

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

A. Toutain, D. Lacombe, J. Battin, 1994, Annales de genetique.

X‐linked dominant chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia

N. Chassaing, B. Gilbert-Dussardier, D. Lacombe, 2005, American journal of medical genetics. Part A.