Battin J - Search Results

1

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

Ressot C, Latour P, Blanquet-Grossard F, Sturtz F, Duthel S, Battin J, Corbillon E, Ollagnon E, Serville F, Vandenberghe A, Dautigny A, Pham-Dinh D. Ressot C, et al. Among authors: battin j. Hum Genet. 1996 Aug;98(2):172-5. doi: 10.1007/s004390050183. Hum Genet. 1996. PMID: 8698335

2

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. Among authors: battin j. 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.

3

[Hemophilia and Duchenne de Boulogne myopathy. Genetics].

Battin J, Serville F. Battin J, et al. Rev Prat. 1994 Sep 15;44(14):1955-60. Rev Prat. 1994. PMID: 7939289 French. No abstract available.

4

[Autosomal chromosome aberrations].

Serville F, Battin J. Serville F, et al. Among authors: battin j. Bord Med. 1971 May;4(5):1373-416. Bord Med. 1971. PMID: 5105683 French. No abstract available.

5

[18 p-syndrome and hypothyroidism].

Battin J, Serville F, Marchand JC. Battin J, et al. Arch Fr Pediatr. 1973 May;30(5):548. Arch Fr Pediatr. 1973. PMID: 4733656 French. No abstract available.

6

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

Battin J, Serville F, Mullon MH, Mateille N. Battin J, et al. J Genet Hum. 1988 Aug;36(4):307-14. J Genet Hum. 1988. PMID: 3221206 French.

7

[Coffin-Lowry syndrome and hyperprolinemia].

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

8

[Neck edema. An echographic sign of trisomy 21 in pregnancy].

Serville F, Battin J, Leng JJ, Vergnaud A, Guilleux MH. Serville F, et al. Among authors: battin j. Arch Fr Pediatr. 1986 Aug-Sep;43(7):487-8. Arch Fr Pediatr. 1986. PMID: 2948475 French.

9

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

Chassaing N, Siani V, Carles D, Delezoide AL, Alberti EM, Battin J, Chateil JF, Gilbert-Dussardier B, Coupry I, Arveiler B, Saura R, Lacombe D. Chassaing N, et al. Among authors: battin j. Am J Med Genet A. 2005 Aug 1;136A(4):307-12. doi: 10.1002/ajmg.a.30570. Am J Med Genet A. 2005. PMID: 16001442

10

[Study of sex determination gene (SRY) in 46,XY gonadal dysgenesis].

Boucekkine C, Vilain E, McElreavey K, Jaubert F, Brauner R, Thibaud E, Battin J, Toublanc JE, Kucheria K, Chaabouni S, et al. Boucekkine C, et al. Among authors: battin j. Ann Endocrinol (Paris). 1994;54(5):315-21. Ann Endocrinol (Paris). 1994. PMID: 8085778 French.

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